What Clinical Study Reports Jobs are in South Africa?
Showing 31 Clinical Study Reports jobs in South Africa
Principal Medical Writer - Clinical Study Reports
2194 Randburg / Remote
Placements24
Posted 9 days ago
Job Viewed
Job Description
About the Role
Our client, a leading pharmaceutical company focused on groundbreaking research, is seeking an experienced Principal Medical Writer to contribute to their global regulatory affairs team, based in Randburg, Gauteng . This senior position is responsible for the planning, writing, and finalization of high-quality clinical study reports (CSRs), Investigator's Brochures (IBs), and other regulatory documents. You will work collaboratively with cross-functional teams, including clinical operations, biostatistics, data management, and regulatory strategy, to ensure accuracy, completeness, and regulatory compliance of all written outputs. The ideal candidate will possess a profound understanding of clinical trial processes, data interpretation, and scientific communication principles. This is an exceptional opportunity to play a critical role in the drug development lifecycle, contributing to regulatory submissions and the successful progression of innovative therapies. We are looking for a highly skilled and detail-oriented writer with a proven track record in medical writing within the pharmaceutical or biotechnology industry, demonstrating a commitment to scientific rigor and clarity. Your expertise will be instrumental in effectively communicating complex clinical data to regulatory authorities and stakeholders.
Key Responsibilities- Author clear, accurate, and scientifically sound Clinical Study Reports (CSRs) for Phase I-IV clinical trials.
- Develop Investigator's Brochures (IBs), protocols, study summaries, and other essential regulatory documents.
- Collaborate closely with clinical investigators, biostatisticians, data managers, and clinical project managers to ensure the accuracy and completeness of data and reports.
- Ensure all medical writing deliverables meet relevant regulatory requirements (e.g., ICH E3) and company standards.
- Review and edit documents authored by other medical writers or team members to ensure quality and consistency.
- Manage multiple writing projects simultaneously, adhering to strict timelines and project milestones.
- Contribute to the development and refinement of medical writing templates and standard operating procedures (SOPs).
- Stay abreast of current industry trends, regulatory guidelines, and best practices in medical writing.
- Serve as a subject matter expert on medical writing for internal and external stakeholders.
- Participate in cross-functional team meetings, providing insights and contributing to strategic discussions.
- Bachelor's or Master's degree in a scientific or healthcare discipline (e.g., Life Sciences, Pharmacy, Medicine, Nursing).
- Minimum of 8 years of experience as a Medical Writer in the pharmaceutical, biotechnology, or contract research organization (CRO) industry.
- Extensive experience authoring Clinical Study Reports (CSRs) in accordance with ICH E3 guidelines.
- Demonstrated ability to interpret and present complex clinical trial data effectively.
- Thorough understanding of clinical trial design, conduct, and regulatory submission processes.
- Exceptional written and verbal communication skills, with a keen eye for detail and scientific accuracy.
- Proficiency in Microsoft Word and experience with document management systems.
- Ability to work independently, manage priorities, and meet demanding deadlines.
- Strong collaborative skills and experience working effectively in cross-functional teams.
- Familiarity with regulatory submission requirements (e.g., FDA, EMA) is essential.
Our client offers a highly competitive salary package, commensurate with experience, and a performance-based bonus program. Comprehensive benefits include excellent medical, dental, and vision insurance, a robust retirement savings plan with employer matching, and life insurance. We provide a generous paid time off (PTO) policy, including vacation, personal days, and holidays, fostering a healthy work-life balance. Opportunities for continuous professional development, including access to training programs, workshops, and scientific conferences, are actively supported. Our client provides a dynamic and collaborative work environment with access to cutting-edge technology. Join a dedicated team of professionals contributing to the development of life-changing medicines in Randburg .
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0
Remote Senior Medical Writer - Clinical Study Reports
Mossel Bay / Remote
Placements24
Posted 6 days ago
Job Viewed
Job Description
About the Role
Our client, a globally recognized leader in pharmaceutical research and development, is seeking a highly experienced and dedicated Senior Medical Writer to join their expanding remote team. This role is crucial for the clear and accurate communication of clinical trial results and other critical research data to regulatory bodies, healthcare professionals, and the scientific community. As a Senior Medical Writer, you will be responsible for authoring, editing, and finalizing a wide range of complex regulatory and scientific documents, including Clinical Study Reports (CSRs), manuscripts, and regulatory submission documents. This is a fully remote position, offering unparalleled flexibility and the opportunity to work from anywhere within suitable time zones to collaborate effectively with global teams. You will be an integral part of a high-performing medical affairs department, contributing to the successful progression of innovative therapies through the development pipeline. Our client is committed to scientific excellence and fostering a collaborative, results-driven remote work culture. This role requires an exceptional command of medical and scientific terminology, a keen eye for detail, and the ability to translate complex data into clear, concise, and compliant documents. You will play a pivotal role in ensuring the integrity and effectiveness of our client's scientific communications.
Key Responsibilities- Author, edit, and finalize high-quality Clinical Study Reports (CSRs), protocols, Investigator's Brochures (IBs), and other clinical documents.
- Prepare manuscripts for submission to peer-reviewed journals and present clinical data effectively.
- Develop responses to regulatory agency queries and prepare submission-ready documents for global health authorities.
- Ensure all documents adhere to company style guides, regulatory guidelines (e.g., ICH-E3), and industry best practices.
- Collaborate closely with cross-functional teams, including clinical operations, biostatistics, regulatory affairs, and project management, to gather information and ensure accuracy.
- Manage multiple document projects simultaneously, adhering to strict timelines and project schedules.
- Review and critique documents authored by other writers or team members.
- Stay updated on therapeutic area advancements, regulatory requirements, and medical writing standards.
- Contribute to the development and maintenance of medical writing templates and SOPs.
- Ensure consistency in messaging and data presentation across all written communications.
- Master's or Ph.D. degree in a life science, medical, or related field.
- A minimum of 7 years of experience in medical writing within the pharmaceutical or biotechnology industry.
- Demonstrated expertise in authoring Clinical Study Reports (CSRs) and other clinical regulatory documents.
- Comprehensive understanding of ICH guidelines (especially ICH E3 for CSRs) and global regulatory submission requirements.
- Exceptional writing, editing, and proofreading skills with a strong command of scientific and medical terminology.
- Proven ability to interpret complex clinical and statistical data.
- Experience working effectively in a remote, global team environment.
- Proficiency with document management systems and collaboration tools.
- Excellent communication, interpersonal, and project management skills.
- Ability to work independently, manage priorities, and meet tight deadlines consistently.
- Detail-oriented with a commitment to producing high-quality, compliant documentation.
Our client offers an exceptionally competitive salary package, reflecting the senior nature and remote flexibility of this role. In addition to a generous annual salary, performance-based bonuses are frequently awarded. As a fully remote employee, you benefit from significant flexibility in managing your work-life balance. Comprehensive health insurance coverage and robust retirement savings plans are provided. Continuous professional development is strongly supported through access to online learning platforms, workshops, and opportunities to attend international medical writing conferences. Our client fosters a truly global and inclusive remote work culture that emphasizes collaboration and mutual respect. Generous paid time off and holiday allowances are provided. Employees also have access to a suite of wellness resources and employee assistance programs. The opportunity for career growth into leadership roles within the medical affairs function is significant. This role allows you to make a substantial impact from the convenience of your own home office.
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1
Registered/ Study Coordinator Clinic Nurse
Cape Town
University of Cape Town Lung Institute
Posted 5 days ago
Job Viewed
Job Description
â What you bring:
Your clinical expertise will help patients better understand, manage, and improve their allergic and immune-related conditions through specialised, evidence-based care.
ð Role Information:
â³ Closing Date: 31 July 2026
Thank you for your interest in this opportunity. Only shortlisted candidates will be contacted. If you havent heard from us within 30 days of the closing date, please consider your application unsuccessful.
ð EMPLOYMENT EQUITY STATEMENT
We are committed to equitable employment practices and diversity in the workplace. Appointments will be made in accordance with the University of Cape Town Lung Institutes Employment Equity Plan.
ð POPIA STATEMENT
Your personal information will be processed in line with the Protection of Personal Information Act (POPIA) and used solely for recruitment purposes, including reference checks. By applying, you consent to this process.
- Degree or Diploma in General Nursing
- Previous phlebotomy experience
- 25 years' clinical experience in a private practice, clinic, or community healthcare setting
- Computer literacy with proficiency in Microsoft Outlook, Excel, Word, and PowerPoint
- Fluency in English and a second language (Afrikaans and/or isiXhosa)
- Excellent interpersonal, communication, organisational, and time management skills
- Ability to work independently while contributing positively within a multidisciplinary clinical team
- Diagnostic testing experience
- Experience within Allergy, Immunology, Dermatology, Respiratory, or Specialist Healthcare environments
- Experience with patient education and long-term treatment support
- Performing clinical assessments, including blood pressure monitoring, lung function testing, skin prick testing, and other diagnostic procedures
- Administering immunotherapy treatments and allergy desensitisation therapies
- Administering bee venom immunotherapy and monitoring patients throughout treatment
- Performing phlebotomy procedures and peripheral IV insertions
- Preparing and managing laboratory specimens for transportation and testing
- Maintaining accurate patient records, laboratory results, and clinical documentation
- Assisting clinicians with interpretation, reporting, and communication of allergy-related results
- Responding to patient queries and supporting ongoing patient care
- Monitoring clinic stock levels and coordinating consumable orders
- Supporting patients through education and treatment planning
Your clinical expertise will help patients better understand, manage, and improve their allergic and immune-related conditions through specialised, evidence-based care.
ð Role Information:
- Fixed Term Contract (6-12 Months)
- Monday to Friday | 40 hours per week
- Based at UCTLI in Observatory,
â³ Closing Date: 31 July 2026
Thank you for your interest in this opportunity. Only shortlisted candidates will be contacted. If you havent heard from us within 30 days of the closing date, please consider your application unsuccessful.
ð EMPLOYMENT EQUITY STATEMENT
We are committed to equitable employment practices and diversity in the workplace. Appointments will be made in accordance with the University of Cape Town Lung Institutes Employment Equity Plan.
ð POPIA STATEMENT
Your personal information will be processed in line with the Protection of Personal Information Act (POPIA) and used solely for recruitment purposes, including reference checks. By applying, you consent to this process.
Is this job a match or a miss?
Apply Now
2
(Senior) Clinical Project Manager - Global Study Leadership
Centurion
IQVIA
Posted 1 day ago
Job Viewed
Job Description
At IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. You'll provide strategic leadership for complex global clinical trials, partnering directly with sponsors and cross-functional teams to deliver studies that accelerate the development of life-changing therapies.
This is an opportunity to lead large-scale, multi-regional studies for some of the world's most innovative pharmaceutical and biotechnology companies while expanding your leadership impact and helping shape the future of clinical research.
**_This position may be filled at either the Clinical Project Manager or Senior Clinical Project Manager level, depending on the selected candidate's relevant experience._**
**Why Join Global Study Leadership?**
Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery models. You'll work on some of the industry's most complex global clinical trials, partnering directly with leading pharmaceutical and biotechnology sponsors across therapeutic areas including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Cell & Gene Therapy, Infectious Disease, Ophthalmology and Women's Health.
Supported by a collaborative global network, flexible ways of working and AI-enabled technology and data-driven insights, you'll have exceptional opportunities to broaden your expertise, expand your leadership impact and accelerate your career within one of the world's leading clinical research organizations.
**What You'll Be Doing**
As the strategic leader of your studies, you'll be accountable for the successful delivery of complex global clinical trials from start-up through close-out, ensuring quality, timeline, budget, regulatory and customer objectives are achieved.
**Key Responsibilities**
+ Lead the delivery of complex global and multi-regional clinical studies, driving operational excellence and successful study outcomes
+ Serve as the primary strategic partner for sponsors, providing leadership, guidance and innovative solutions to drive successful study outcomes
+ Provide leadership and direction to cross-functional teams across regions, fostering collaboration, accountability and high performance
+ Oversee study timelines, budgets, quality, risks, financial performance and operational delivery to ensure study success
+ Drive proactive risk management, issue resolution, decision-making and stakeholder alignment throughout the study lifecycle
+ Ensure studies are delivered in compliance with ICH-GCP, regulatory requirements and contractual commitments
**What We're Looking For**
+ Bachelor's degree in Life Sciences, Healthcare or a related scientific discipline
+ 7+ years of clinical research experience, including significant project management experience leading global or multi-regional clinical trials within a CRO, pharmaceutical or biotechnology environment
+ Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements
+ Proven success leading cross-functional teams and managing study delivery, including timelines, budgets, quality, risks and operational performance
+ Demonstrated ability to build trusted sponsor relationships and effectively manage senior stakeholders in a global environment
+ Exceptional leadership, communication, problem-solving and decision-making skills
+ Passion for advancing clinical research and improving patient outcomes
**Build Your Future with IQVIA**
If you're looking for a role that combines global exposure, strategic leadership, sponsor partnership and meaningful work, we'd love to hear from you. At IQVIA, you'll have the opportunity to work on high-profile global studies, collaborate with industry-leading sponsors, leverage cutting-edge technology and build a rewarding career with one of the world's leading clinical research organizations, all while helping bring innovative treatments to patients faster.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This is an opportunity to lead large-scale, multi-regional studies for some of the world's most innovative pharmaceutical and biotechnology companies while expanding your leadership impact and helping shape the future of clinical research.
**_This position may be filled at either the Clinical Project Manager or Senior Clinical Project Manager level, depending on the selected candidate's relevant experience._**
**Why Join Global Study Leadership?**
Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery models. You'll work on some of the industry's most complex global clinical trials, partnering directly with leading pharmaceutical and biotechnology sponsors across therapeutic areas including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Cell & Gene Therapy, Infectious Disease, Ophthalmology and Women's Health.
Supported by a collaborative global network, flexible ways of working and AI-enabled technology and data-driven insights, you'll have exceptional opportunities to broaden your expertise, expand your leadership impact and accelerate your career within one of the world's leading clinical research organizations.
**What You'll Be Doing**
As the strategic leader of your studies, you'll be accountable for the successful delivery of complex global clinical trials from start-up through close-out, ensuring quality, timeline, budget, regulatory and customer objectives are achieved.
**Key Responsibilities**
+ Lead the delivery of complex global and multi-regional clinical studies, driving operational excellence and successful study outcomes
+ Serve as the primary strategic partner for sponsors, providing leadership, guidance and innovative solutions to drive successful study outcomes
+ Provide leadership and direction to cross-functional teams across regions, fostering collaboration, accountability and high performance
+ Oversee study timelines, budgets, quality, risks, financial performance and operational delivery to ensure study success
+ Drive proactive risk management, issue resolution, decision-making and stakeholder alignment throughout the study lifecycle
+ Ensure studies are delivered in compliance with ICH-GCP, regulatory requirements and contractual commitments
**What We're Looking For**
+ Bachelor's degree in Life Sciences, Healthcare or a related scientific discipline
+ 7+ years of clinical research experience, including significant project management experience leading global or multi-regional clinical trials within a CRO, pharmaceutical or biotechnology environment
+ Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements
+ Proven success leading cross-functional teams and managing study delivery, including timelines, budgets, quality, risks and operational performance
+ Demonstrated ability to build trusted sponsor relationships and effectively manage senior stakeholders in a global environment
+ Exceptional leadership, communication, problem-solving and decision-making skills
+ Passion for advancing clinical research and improving patient outcomes
**Build Your Future with IQVIA**
If you're looking for a role that combines global exposure, strategic leadership, sponsor partnership and meaningful work, we'd love to hear from you. At IQVIA, you'll have the opportunity to work on high-profile global studies, collaborate with industry-leading sponsors, leverage cutting-edge technology and build a rewarding career with one of the world's leading clinical research organizations, all while helping bring innovative treatments to patients faster.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Is this job a match or a miss?
Apply Now
3
Senior Clinical Data Science Programmer
Johannesburg
ICON Clinical Research
Posted 9 days ago
Job Viewed
Job Description
Senior Clinical Data Science Programmer (Clinical SAS Listings)
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Are you an experienced **Clinical SAS Listings Programmer** with 3+ years of experience developing and maintaining clinical study listings looking for your next opportunity?
ICON is growing and we're looking for talented professionals to join our Clinical Data Science team in a fully remote role. This is an exciting opportunity for an experienced programmer with strong expertise in **Clinical Study Listings, including DM Listings and Reconciliation Listings** , to work in a client-facing role and deliver high-quality clinical data science and programming solutions that support clinical development programmes across a global portfolio.
**What You Will Be Doing**
+ Develop, validate, and maintain Clinical Study Listings, including DM Listings, Reconciliation Listings, and other study-specific listings.
+ Ensure study listings are configured, delivered, and maintained in line with agreed timelines and quality expectations.
+ Manage clinical study listings in compliance with clinical standards to support the successful execution of clinical trials.
+ Serve as the subject matter expert for Clinical Study Listings, providing support, troubleshooting, and maintenance activities.
+ Partner directly with stakeholders, providing technical expertise and acting as a key contact for programming-related activities.
+ Participate in client meetings, delivering updates, presenting outputs, and supporting decision-making throughout the study lifecycle.
+ Provide guidance on programming best practices, coding standards, validation approaches, and data quality controls.
**You Will Have/Be**
+ Bachelor's degree in Life Sciences, Computer Science, Statistics, or a related discipline.
+ Minimum 3 years of experience developing, validating, and maintaining Clinical SAS Listings.
+ Demonstrated experience producing DM Listings, Reconciliation Listings, and other clinical study listings.
+ Strong proficiency in SAS and experience with programming languages such as R, Rave Custom Functions, and Python.
+ Understanding of CDISC standards and clinical reporting best practices.
+ Excellent verbal and written communication skills.
+ Ability to work independently in a remote environment while managing multiple priorities and deadlines.
\#LI-RD1
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Are you an experienced **Clinical SAS Listings Programmer** with 3+ years of experience developing and maintaining clinical study listings looking for your next opportunity?
ICON is growing and we're looking for talented professionals to join our Clinical Data Science team in a fully remote role. This is an exciting opportunity for an experienced programmer with strong expertise in **Clinical Study Listings, including DM Listings and Reconciliation Listings** , to work in a client-facing role and deliver high-quality clinical data science and programming solutions that support clinical development programmes across a global portfolio.
**What You Will Be Doing**
+ Develop, validate, and maintain Clinical Study Listings, including DM Listings, Reconciliation Listings, and other study-specific listings.
+ Ensure study listings are configured, delivered, and maintained in line with agreed timelines and quality expectations.
+ Manage clinical study listings in compliance with clinical standards to support the successful execution of clinical trials.
+ Serve as the subject matter expert for Clinical Study Listings, providing support, troubleshooting, and maintenance activities.
+ Partner directly with stakeholders, providing technical expertise and acting as a key contact for programming-related activities.
+ Participate in client meetings, delivering updates, presenting outputs, and supporting decision-making throughout the study lifecycle.
+ Provide guidance on programming best practices, coding standards, validation approaches, and data quality controls.
**You Will Have/Be**
+ Bachelor's degree in Life Sciences, Computer Science, Statistics, or a related discipline.
+ Minimum 3 years of experience developing, validating, and maintaining Clinical SAS Listings.
+ Demonstrated experience producing DM Listings, Reconciliation Listings, and other clinical study listings.
+ Strong proficiency in SAS and experience with programming languages such as R, Rave Custom Functions, and Python.
+ Understanding of CDISC standards and clinical reporting best practices.
+ Excellent verbal and written communication skills.
+ Ability to work independently in a remote environment while managing multiple priorities and deadlines.
\#LI-RD1
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
Is this job a match or a miss?
Apply Now
4
Job Description
Clinical Data Risk Analyst
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Clinical Data Risk Analyst at ICON, you will identify and mitigating risks associated with clinical trial data. You will contribute to the overall success of our clinical programs by employing risk assessment methodologies to ensure data integrity and compliance with regulatory standards.
**What You Will Do:**
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
+ Conducting risk assessments on clinical trial data to identify potential issues and recommend mitigation strategies.
+ Collaborating with cross-functional teams to develop and implement risk management plans and protocols.
+ Monitoring data quality and integrity throughout the trial process, reporting findings to stakeholders.
+ Utilizing statistical analysis and visualization tools to communicate risk-related insights effectively.
+ Supporting the preparation of risk management documentation for regulatory submissions and audits.
**Your Profile:**
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
+ Degree in statistics, life sciences, or a related field.
+ 3 years experience in within a clinical research environment.
+ Strong analytical and technical skills.
+ Attention to detail and a proactive approach to identifying and addressing data risks.
+ Effective communication skills, with the ability to collaborate across diverse teams and convey complex information clearly.
\#LI-RD1
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Clinical Data Risk Analyst at ICON, you will identify and mitigating risks associated with clinical trial data. You will contribute to the overall success of our clinical programs by employing risk assessment methodologies to ensure data integrity and compliance with regulatory standards.
**What You Will Do:**
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
+ Conducting risk assessments on clinical trial data to identify potential issues and recommend mitigation strategies.
+ Collaborating with cross-functional teams to develop and implement risk management plans and protocols.
+ Monitoring data quality and integrity throughout the trial process, reporting findings to stakeholders.
+ Utilizing statistical analysis and visualization tools to communicate risk-related insights effectively.
+ Supporting the preparation of risk management documentation for regulatory submissions and audits.
**Your Profile:**
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
+ Degree in statistics, life sciences, or a related field.
+ 3 years experience in within a clinical research environment.
+ Strong analytical and technical skills.
+ Attention to detail and a proactive approach to identifying and addressing data risks.
+ Effective communication skills, with the ability to collaborate across diverse teams and convey complex information clearly.
\#LI-RD1
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
Is this job a match or a miss?
Apply Now
5
Global Study Manager - Single Sponsor dedicated (in EMEA)
Bloemfontein
IQVIA
Posted today
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Job Description
**Job Overview**
The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving.
The GSM works cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with Global Study Director (GSD) or Global Study Associate Director (GSAD) in delegated aspects of clinical study execution in accordance with the Delivery Model.
**Essential Functions**
In partnership with client's team,
- Leads/contributes to the preparation of delegated study documents (e.g., Informed Consent Form, master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.).
- Maintains and facilitates interactions with internal functions and external functions including the CROs and other external service providers to ensure an efficient study delivery to time, costs and quality objectives.
- Contributes to the planning and conduct of internal and external meetings (e.g., Investigators'/Monitors' meeting).
- Ensures the supply of Investigational product and study materials by liaising with Clinical Supply Chain or external service providers as appropriate.
- Proactively contributes to risk and issue identification, development of mitigation and/or action plans for identified risks and issues.
- Ensures that all study documents in scope of GSM's responsibilities are complete and verified for quality in Trial Master File.
- Supports GSD and/or GSAD with budget management, such as external service provider invoice reconciliation.
- Adheres to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international guidelines such as ICH/GCP to ensure study is inspection ready at all times.
- Supports GSD and/or GSAD with overall project management as per agreed delegation.
- For outsourced studies, supports GSD and/or GSAD in management of the CRO Project Manager to ensure study delivery according to agreed timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study, in accordance with
Internal BioPharmaceuticals Clinical Operations Job Description
relevant client's SOPs and guidelines (e.g., description of services and transfer of obligations)
- Take on assignments on non-drug project work in process improvements and/or leading improvement projects as discussed and agreed upon with their manager
**Qualifications**
- University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.
- Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably of at least 3 years.
- Knowledge of clinical development / drug development process in various phases of development and therapy areas
- Excellent knowledge of international guidelines ICH/GCP
- Excellent communication and relationship building skills, including external service provider management skills
- Good project management skills
- Demonstrated ability to collaborate as well as work independently
- Demonstrated leadership skills
- Computer proficiency, advanced computer skills in day-to-day tasks
- Excellent verbal and written communication in English
**Please note this role is not eligible for the UK visa sponsorship.**
_Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered._
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is 171.500,00 zł - 404.600,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving.
The GSM works cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with Global Study Director (GSD) or Global Study Associate Director (GSAD) in delegated aspects of clinical study execution in accordance with the Delivery Model.
**Essential Functions**
In partnership with client's team,
- Leads/contributes to the preparation of delegated study documents (e.g., Informed Consent Form, master Clinical Study Agreement etc), and external service provider related documents (specifications, study specific procedures, descriptions, presentations etc.).
- Maintains and facilitates interactions with internal functions and external functions including the CROs and other external service providers to ensure an efficient study delivery to time, costs and quality objectives.
- Contributes to the planning and conduct of internal and external meetings (e.g., Investigators'/Monitors' meeting).
- Ensures the supply of Investigational product and study materials by liaising with Clinical Supply Chain or external service providers as appropriate.
- Proactively contributes to risk and issue identification, development of mitigation and/or action plans for identified risks and issues.
- Ensures that all study documents in scope of GSM's responsibilities are complete and verified for quality in Trial Master File.
- Supports GSD and/or GSAD with budget management, such as external service provider invoice reconciliation.
- Adheres to global clinical processes, procedural documents, applicable Quality & Compliance manual documents and international guidelines such as ICH/GCP to ensure study is inspection ready at all times.
- Supports GSD and/or GSAD with overall project management as per agreed delegation.
- For outsourced studies, supports GSD and/or GSAD in management of the CRO Project Manager to ensure study delivery according to agreed timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study, in accordance with
Internal BioPharmaceuticals Clinical Operations Job Description
relevant client's SOPs and guidelines (e.g., description of services and transfer of obligations)
- Take on assignments on non-drug project work in process improvements and/or leading improvement projects as discussed and agreed upon with their manager
**Qualifications**
- University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.
- Relevant experience from within the pharmaceutical industry or similar organization or academic experience, preferably of at least 3 years.
- Knowledge of clinical development / drug development process in various phases of development and therapy areas
- Excellent knowledge of international guidelines ICH/GCP
- Excellent communication and relationship building skills, including external service provider management skills
- Good project management skills
- Demonstrated ability to collaborate as well as work independently
- Demonstrated leadership skills
- Computer proficiency, advanced computer skills in day-to-day tasks
- Excellent verbal and written communication in English
**Please note this role is not eligible for the UK visa sponsorship.**
_Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered._
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is 171.500,00 zł - 404.600,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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6
Job Description
We are looking for a motivated and clinically confident Dietitian to join our hospital-based team, working mainly across Life Hilton Hospital and Lenmed Hospital, as well as surrounding units.
The role involves providing high-quality clinical nutrition care to a wide range of patients, including ICU, surgical, medical, nephrology, elderly care, oncology, and metabolic disease patients. The Dietitian will be expected to assess patients, develop appropriate nutrition care plans, monitor progress, and communicate clearly with doctors, nursing staff, patients, and families.
The candidate will work closely within the multidisciplinary team, including participation in regular ICU MDT ward rounds, ensuring that nutrition forms an active and valuable part of patient management.
Key responsibilities include:
Nutritional assessment and management of hospital inpatients.
ICU nutrition support, including enteral and parenteral nutrition considerations.
Management of surgical, medical, nephrology, geriatric, and metabolic disease patients.
Clear communication with doctors, nurses, patients, and families.
Participation in MDT discussions and ICU ward rounds.
Accurate documentation, follow-up, and continuity of patient care.
Building strong professional relationships with referring doctors and hospital teams.
Promoting excellent patient-centered nutrition care across the hospitals.
Requirements & Qualifications:
Bachelor’s or Master’s degree in Nutrition & Dietetics or related field
Registered Dietician with HPCSA
Minimum 3-5 years of clinical experience
Strong communication, teamwork, and counselling skills
Must have own vehicle and valid license - NB
The ideal candidate should be professional, compassionate, organised, clinically curious, and comfortable working in a busy hospital environment. Strong communication skills and the ability to work well within a multidisciplinary team are essential.
As part of our commitment to developing clinical excellence, the successful Dietitian will receive additional clinical training through Critical Point, facilitated by Dr Lauryn Hill. This training covers critical care nutrition, nephrology nutrition, and surgical nutrition. Upon completion, the Dietitian will become accredited through Critical Point as a Dietitian who has received advanced clinical training. The full cost of this training is borne by the practice as part of our commitment to upskilling our clinical team and enhancing the level of care provided to our patients.
This is a valuable opportunity for a Dietitian who wants to grow in the hospital clinical nutrition space and be part of a dynamic, supportive private practice team.
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7
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Internship **South Africa**
Are you a recent graduate who would like to take his\her first steps within a dynamic clinical research organization? Are you interested in learning fundamental skills to start your career effectively?
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**How will you make an impact?**
The 12-month internship in Clinical Operations is designed to offer you the opportunity to develop insight into clinical research, master your skills while conducting meaningful work within the team. The programme framework is crafted to allow you to grow professionally, learning invaluable skills to help you kick start your career!
**What you will do?**
As part of Clinical Operations, you will work closely as a team, providing support and ideas for day to day activities. Your engagement and level of dedication will ensure that our project teams would receive the administrative and technical support they need. You will have an ambassador who will help you navigate through our organization and processes and receive the best support, which will ensure you are on your way to reaching your goals.
Being part of the Clinical Operations team, you will be introduced to many diverse parts of the company. You will have a wide portfolio of exciting tasks to complete. Plus test your natural curiosity in providing administrative and technical support to the team proactively, educating yourself about the clinical research industry and master your skills to measure your business progress.
**How will you get here?**
+ You possess a health science degree and recently graduated (Within the last 2 years)
+ You have not previously been employed
+ You are looking for an entry level position
+ You enjoy working in a team
+ You have excellent administration and organization skills and the ability to prioritize and handle various tasks timeously
+ You are results oriented
+ You demonstrate a positive demeanor and desire to succeed
+ You exhibit a high degree of flexibility in adapting to a constantly evolving business environment
+ You have English proficiency
_In line with our Employment Equity Plan, preference may be given to suitably qualified male candidates from designated groups (African, Indian, and Coloured) in accordance with the Employment Equity Act. All applications will be considered on the basis of skills, qualifications, and experience._
**Work Environment:**
At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD Clinical Research Services you will benefit from an award-winning learning and development programme, ensuring you reach your potential.
Our Mission is to enable our customers to make the world healthier, cleaner and safer.
As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Internship **South Africa**
Are you a recent graduate who would like to take his\her first steps within a dynamic clinical research organization? Are you interested in learning fundamental skills to start your career effectively?
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**How will you make an impact?**
The 12-month internship in Clinical Operations is designed to offer you the opportunity to develop insight into clinical research, master your skills while conducting meaningful work within the team. The programme framework is crafted to allow you to grow professionally, learning invaluable skills to help you kick start your career!
**What you will do?**
As part of Clinical Operations, you will work closely as a team, providing support and ideas for day to day activities. Your engagement and level of dedication will ensure that our project teams would receive the administrative and technical support they need. You will have an ambassador who will help you navigate through our organization and processes and receive the best support, which will ensure you are on your way to reaching your goals.
Being part of the Clinical Operations team, you will be introduced to many diverse parts of the company. You will have a wide portfolio of exciting tasks to complete. Plus test your natural curiosity in providing administrative and technical support to the team proactively, educating yourself about the clinical research industry and master your skills to measure your business progress.
**How will you get here?**
+ You possess a health science degree and recently graduated (Within the last 2 years)
+ You have not previously been employed
+ You are looking for an entry level position
+ You enjoy working in a team
+ You have excellent administration and organization skills and the ability to prioritize and handle various tasks timeously
+ You are results oriented
+ You demonstrate a positive demeanor and desire to succeed
+ You exhibit a high degree of flexibility in adapting to a constantly evolving business environment
+ You have English proficiency
_In line with our Employment Equity Plan, preference may be given to suitably qualified male candidates from designated groups (African, Indian, and Coloured) in accordance with the Employment Equity Act. All applications will be considered on the basis of skills, qualifications, and experience._
**Work Environment:**
At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD Clinical Research Services you will benefit from an award-winning learning and development programme, ensuring you reach your potential.
Our Mission is to enable our customers to make the world healthier, cleaner and safer.
As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Apply Now
8