What Clinical Trial Manager Jobs are in South Africa?
Showing 527 Clinical Trial Manager jobs in South Africa
Job Description
**Clinical Trial Manager - IQVIA Biotech**
*** _Please note: due to sponsor requirements for the role only candidates based in the listed location/s and with previous Global CTM experience will be considered. Any applications from candidates based outside of these locations will not be considered._
**Job Overview**
Clinical Trial Managers (CTM) are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The CTM is a member of the core project team responsible for clinical delivery of full service, large, multi-regional studies to meet contractual requirements and in accordance with (Standard Operating Procedures) SOPs, policies and practices.
**Essential Functions**
- Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).
- Accountable for meeting projects' recruitment targets and ensuring appropriate recruitment strategies are in place.
- Contribute to the development of the project risk mitigation plan. Manage clinical risks through the project lifecycle.
- Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.
- Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.
- Work as the primary CTM alongside other CTMs to deliver large, global trials.
- Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
- Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.
- Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.
- Conduct regular team meetings and communicate appropriately to achieve objectives.
- Support professional development by providing feedback to clinical team line managers on performance relative to project tasks to support professional development.
- Adopt corporate initiatives and changes and serve as a change advocate when necessary.
- May contribute to the development of the clinical delivery strategy for business proposals. Participate in bid defense preparations and meetings. Develop and present Clinical Operation plan in partnership with Business Development and Project Leadership.
- May mentor and coach new peers as they assimilate into this role.
- May attend site visits as applicable in support of project delivery.
**Qualifications**
- Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required
**Experience**
- Ideally at least 5 years experience in clinical trial management or equivalent combination of education, training and experience.
- Requires consolidated knowledge of Project management practices and terminology.
- Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Requires broad protocol knowledge and therapeutic knowledge.; Req
- Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.
- Requires understanding of project finances.
- Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements
i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;
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
*** _Please note: due to sponsor requirements for the role only candidates based in the listed location/s and with previous Global CTM experience will be considered. Any applications from candidates based outside of these locations will not be considered._
**Job Overview**
Clinical Trial Managers (CTM) are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. The CTM is a member of the core project team responsible for clinical delivery of full service, large, multi-regional studies to meet contractual requirements and in accordance with (Standard Operating Procedures) SOPs, policies and practices.
**Essential Functions**
- Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).
- Accountable for meeting projects' recruitment targets and ensuring appropriate recruitment strategies are in place.
- Contribute to the development of the project risk mitigation plan. Manage clinical risks through the project lifecycle.
- Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.
- Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.
- Work as the primary CTM alongside other CTMs to deliver large, global trials.
- Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.
- Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.
- Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.
- Conduct regular team meetings and communicate appropriately to achieve objectives.
- Support professional development by providing feedback to clinical team line managers on performance relative to project tasks to support professional development.
- Adopt corporate initiatives and changes and serve as a change advocate when necessary.
- May contribute to the development of the clinical delivery strategy for business proposals. Participate in bid defense preparations and meetings. Develop and present Clinical Operation plan in partnership with Business Development and Project Leadership.
- May mentor and coach new peers as they assimilate into this role.
- May attend site visits as applicable in support of project delivery.
**Qualifications**
- Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required
**Experience**
- Ideally at least 5 years experience in clinical trial management or equivalent combination of education, training and experience.
- Requires consolidated knowledge of Project management practices and terminology.
- Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Requires broad protocol knowledge and therapeutic knowledge.; Req
- Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.
- Requires understanding of project finances.
- Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements
i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;
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
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0
Job Description
About the Role
Our client, a prominent pharmaceutical organization, is actively seeking an experienced and detail-oriented Clinical Trial Manager to oversee critical clinical research operations in Tembisa, Gauteng . This role is integral to bringing life-changing therapies to patients by ensuring the successful execution of clinical trials according to stringent regulatory standards and internal protocols. The Clinical Trial Manager will be responsible for the planning, execution, and completion of clinical studies, managing all aspects from site selection and initiation to monitoring, data collection, and close-out. This hybrid position offers the flexibility to balance home-based work with essential on-site activities, fostering a productive and adaptable work environment. You will play a pivotal role in advancing our client's drug development pipeline.
Key Responsibilities- Develop and manage clinical trial protocols, study plans, and budgets.
- Oversee the selection, training, and management of clinical investigative sites and site staff.
- Ensure compliance with Good Clinical Practice (GCP), regulatory requirements (e.g., SAHPRA), and company SOPs.
- Monitor trial progress, identify risks, and implement mitigation strategies.
- Manage the collection, verification, and management of clinical trial data.
- Act as the primary point of contact for investigators, site personnel, and other external stakeholders.
- Coordinate with internal departments such as regulatory affairs, data management, and biostatistics.
- Prepare and present study updates to senior management and project teams.
- Ensure timely submission of study-related documents and reports.
- Lead and mentor clinical research associates (CRAs) and other study team members.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field. A Master's degree is advantageous.
- Minimum of 4 years of progressive experience in clinical trial management within the pharmaceutical industry or a CRO.
- Demonstrated knowledge of clinical trial processes, regulatory requirements (ICH-GCP, local regulations).
- Proven ability to manage multiple clinical trials simultaneously.
- Strong project management, organizational, and leadership skills.
- Excellent interpersonal, communication, and negotiation skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work effectively in a hybrid work model, demonstrating self-discipline and excellent time management.
- Willingness to travel to investigative sites as required.
- Experience in Phase II and Phase III trials is preferred.
Our client is committed to providing a rewarding employment experience, offering a competitive salary, annual bonus opportunities, comprehensive health insurance, and a retirement savings plan. Employees receive generous annual leave, sick leave, and study leave. Professional development is highly encouraged through access to industry conferences, training courses, and opportunities for career progression. The company promotes a positive and inclusive work culture. This role offers the advantage of a hybrid work arrangement, allowing for a healthy work-life balance while contributing to impactful pharmaceutical research in Tembisa, Gauteng .
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1
Job Description
About the Role Our client, a prominent pharmaceutical company, is seeking a skilled and experienced Clinical Trial Manager to oversee the execution of clinical trials. This role, based in **George, Western Cape**, offers a hybrid work arrangement, allowing for a blend of remote flexibility and in-office collaboration. You will be responsible for the planning, implementation, and successful completion of clinical trials in accordance with regulatory requirements and company standards. This position is integral to bringing new and improved treatments to patients, requiring meticulous attention to detail and strong leadership capabilities. You will manage all aspects of trial operations, ensuring data integrity, subject safety, and adherence to protocols. The objective is to ensure trials are conducted efficiently and ethically, contributing to the advancement of pharmaceutical innovation. Key Responsibilities
- Develop and manage clinical trial protocols, budgets, and timelines.
- Oversee site selection, initiation, monitoring, and close-out activities.
- Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and other applicable guidelines.
- Manage and mentor clinical research staff, including Clinical Research Associates (CRAs).
- Liaise with investigators, site staff, regulatory authorities, and internal stakeholders.
- Monitor trial progress, identify risks, and implement mitigation strategies.
- Ensure the quality and integrity of clinical trial data through effective monitoring and data management oversight.
- Manage vendor relationships, such as Contract Research Organizations (CROs).
- Prepare and present trial status reports to senior management and relevant committees.
- Contribute to the development of clinical development strategies and regulatory submissions.
- Bachelor's degree in a life science, nursing, or a related field; advanced degree preferred.
- Minimum of 5 years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
- Demonstrated experience in managing multi-center clinical trials, preferably in South Africa.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven leadership and team management skills, with experience managing CRAs.
- Excellent project management skills, with the ability to manage multiple priorities and deadlines.
- Strong communication, negotiation, and interpersonal skills.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Ability to work effectively in a hybrid work environment, demonstrating strong self-management skills.
- A proactive approach to problem-solving and decision-making.
- Competitive remuneration package.
- Hybrid work model offering flexibility.
- Opportunities for professional growth and career advancement within a growing company.
- Comprehensive health and wellness benefits.
- Contribute to the development of innovative pharmaceutical products.
- Dynamic and collaborative work environment.
- Relocation assistance may be considered for exceptional candidates.
- Exposure to international clinical trial operations.
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2
Clinical Trial Manager - Pharmaceutical Research
0700 Polokwane / Remote
Placements24
Posted 9 days ago
Job Viewed
Job Description
About the Role Our client, a dynamic and growing pharmaceutical research organization, is seeking an experienced Clinical Trial Manager to oversee complex clinical trials in **Polokwane**. This role involves the end-to-end management of clinical trial activities, ensuring they are conducted on time, within budget, and in compliance with all regulatory requirements and protocols. You will lead a multidisciplinary team, coordinate with investigative sites, and manage vendor relationships. The ideal candidate will possess strong leadership, project management, and communication skills, coupled with a comprehensive understanding of clinical trial operations. This hybrid position offers a unique opportunity to contribute to groundbreaking medical research in **Polokwane, Limpopo**, while maintaining a flexible work-life balance. Key Responsibilities
- Manage all aspects of clinical trial execution, from initiation to close-out, ensuring adherence to study protocols and regulatory guidelines.
- Develop and manage clinical trial budgets and timelines.
- Oversee the selection, training, and performance of clinical trial sites and investigators.
- Ensure timely and accurate data collection, management, and reporting.
- Lead and motivate cross-functional trial teams, fostering a collaborative environment.
- Manage relationships with vendors and external service providers (e.g., CROs, central labs).
- Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements.
- Prepare and present regular study updates to senior management and stakeholders.
- Identify and mitigate risks associated with clinical trial conduct.
- Contribute to the development of clinical trial protocols and study-related documents.
- Bachelor's degree in a life science, healthcare, or related field. Master's degree or equivalent is preferred.
- Minimum of 7 years of experience in clinical research, with at least 3 years in a clinical trial management or project management role.
- Proven experience managing Phase I-IV clinical trials across various therapeutic areas.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements (e.g., SAHPRA).
- Demonstrated leadership and team management skills.
- Strong project management skills, including budgeting, planning, and risk management.
- Excellent organizational, problem-solving, and decision-making abilities.
- Outstanding written and verbal communication skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Willingness to travel as needed for site visits and team meetings within **Polokwane** and broader region.
- Competitive salary with performance-based incentives.
- Comprehensive health insurance and retirement savings plan.
- Generous opportunities for professional development and training.
- Flexible hybrid work arrangement.
- The chance to lead impactful research projects in **Polokwane** and contribute to medical advancements.
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3
(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
4
Job Description
Parexel is currently seeking a Clinical Data Manager to join us in South Africa, dedicated to a single sponsor.
This role will be responsible for performing Data Management activities that support the sponsor's commercial and development projects worldwide. The successful candidate will participate as an active member of a multi-disciplinary team to plan and execute the Data Management tasks required for phase I - IV studies. The Clinical Data Manager has a broad, fundamental knowledge of the data management process and can perform most required tasks with minimal guidance.
Working as a Clinical Data Manager at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Expect exciting professional challenges in inspiring studies, but with time for your outside life.
This will be a fully remote home-based position. RAVE experience is strongly preferred.
**Responsibilities**
+ Lead a small clinical study or a co-lead a larger study or studies with moderate guidance.
+ Be able to support several clinical studies with minimal guidance.
+ Manage and monitor the progress of data management activities with CROs or other vendors on assigned studies.
+ Review protocols for appropriate data capture including electronic Case Report Form (eCRF) design.
+ Be able to perform a thoroughly detailed review of eCRF data requirements.
+ Interact with CRAs, programmers, study managers and statisticians in designing eCRFs and creating the annotated eCRF and CRF completion guidelines.
+ Develop data edit check specifications and run data listings as required.
+ Coordinate the design and testing of Electronic Data Capture (EDC) systems according to company standards. Able to resolve EDC system issues with team members.
+ Develop the Data Management Plan for a clinical study.
+ Able to review and provide feedback to the clinical team on other study documents e.g. Clinical Monitoring plans, Statistical analysis plans and vendor specifications.
+ Enter data queries into the EDC system to be resolved at investigational sites and manage the resolution of those queries.
+ Perform reconciliation of header data from external data sources against the clinical database.
+ Perform Serious Adverse Event reconciliation activities according to SOPs and guidelines.
+ Assist in database upgrades/migrations including performing User Acceptance Testing.
+ Able to maintain study workbooks and data management files.
+ Perform database lock and freeze activities per company SOPs.
+ Participate in regular team meetings and provide input when appropriate.
+ Provide input into the development of data management SOPs, Work Instructions, and process documents.
+ Assist with the training of new employees and/or contractors.
+ Collaborates with cross-functional teams to design and implement effective data collection strategies, ensuring high-quality data capture and timely resolution of data queries throughout the clinical trial lifecycle.
**Here are a few requirements specific to this advertised role.**
+ Bachelor's Degree required (master's preferred), preferably in the scientific/healthcare field.
+ At least five years' experience in Data Management for the pharmaceutical/biotechnology industry.
+ Understanding of the scope and focus of Phase I - IV clinical studies, and a proven ability to perform some of the core Data Management tasks and interact with vendors.
+ An understanding of regulatory guidelines and industry standards (e.g., ICH/FDA guidance, CDISC standards, GCDMP, 21 CFR 11, MedDRA, WHO Drug Dictionaries, etc.) and their application to Data Management practice.
+ Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors.
+ Detail-oriented with a proven ability to multitask and work independently. Excellent time management and organizational skills, with highly developed problem-solving and analytical abilities.
+ Strong English language written and verbal communication skills.
+ Able to travel to meetings or training seminars on occasion.
+ Possesses solid computer system and technical skills with a strong ability to learn multiple computer applications. Prior experience with different Data Management systems and technologies, and Electronic Data Capture systems is desirable.
+ Experience and understanding of the Oncology or CNS therapeutic area and with Phase III pivotal studies are desirable.
We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.
**Who are Parexel**
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today's top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
You'll be an influential member of the wider team.
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Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
This role will be responsible for performing Data Management activities that support the sponsor's commercial and development projects worldwide. The successful candidate will participate as an active member of a multi-disciplinary team to plan and execute the Data Management tasks required for phase I - IV studies. The Clinical Data Manager has a broad, fundamental knowledge of the data management process and can perform most required tasks with minimal guidance.
Working as a Clinical Data Manager at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Expect exciting professional challenges in inspiring studies, but with time for your outside life.
This will be a fully remote home-based position. RAVE experience is strongly preferred.
**Responsibilities**
+ Lead a small clinical study or a co-lead a larger study or studies with moderate guidance.
+ Be able to support several clinical studies with minimal guidance.
+ Manage and monitor the progress of data management activities with CROs or other vendors on assigned studies.
+ Review protocols for appropriate data capture including electronic Case Report Form (eCRF) design.
+ Be able to perform a thoroughly detailed review of eCRF data requirements.
+ Interact with CRAs, programmers, study managers and statisticians in designing eCRFs and creating the annotated eCRF and CRF completion guidelines.
+ Develop data edit check specifications and run data listings as required.
+ Coordinate the design and testing of Electronic Data Capture (EDC) systems according to company standards. Able to resolve EDC system issues with team members.
+ Develop the Data Management Plan for a clinical study.
+ Able to review and provide feedback to the clinical team on other study documents e.g. Clinical Monitoring plans, Statistical analysis plans and vendor specifications.
+ Enter data queries into the EDC system to be resolved at investigational sites and manage the resolution of those queries.
+ Perform reconciliation of header data from external data sources against the clinical database.
+ Perform Serious Adverse Event reconciliation activities according to SOPs and guidelines.
+ Assist in database upgrades/migrations including performing User Acceptance Testing.
+ Able to maintain study workbooks and data management files.
+ Perform database lock and freeze activities per company SOPs.
+ Participate in regular team meetings and provide input when appropriate.
+ Provide input into the development of data management SOPs, Work Instructions, and process documents.
+ Assist with the training of new employees and/or contractors.
+ Collaborates with cross-functional teams to design and implement effective data collection strategies, ensuring high-quality data capture and timely resolution of data queries throughout the clinical trial lifecycle.
**Here are a few requirements specific to this advertised role.**
+ Bachelor's Degree required (master's preferred), preferably in the scientific/healthcare field.
+ At least five years' experience in Data Management for the pharmaceutical/biotechnology industry.
+ Understanding of the scope and focus of Phase I - IV clinical studies, and a proven ability to perform some of the core Data Management tasks and interact with vendors.
+ An understanding of regulatory guidelines and industry standards (e.g., ICH/FDA guidance, CDISC standards, GCDMP, 21 CFR 11, MedDRA, WHO Drug Dictionaries, etc.) and their application to Data Management practice.
+ Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors.
+ Detail-oriented with a proven ability to multitask and work independently. Excellent time management and organizational skills, with highly developed problem-solving and analytical abilities.
+ Strong English language written and verbal communication skills.
+ Able to travel to meetings or training seminars on occasion.
+ Possesses solid computer system and technical skills with a strong ability to learn multiple computer applications. Prior experience with different Data Management systems and technologies, and Electronic Data Capture systems is desirable.
+ Experience and understanding of the Oncology or CNS therapeutic area and with Phase III pivotal studies are desirable.
We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.
**Who are Parexel**
Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.
We supported the trials of most of today's top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.
You'll be an influential member of the wider team.
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Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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5
Remote Pharmaceutical Clinical Trial Manager
7600 Stellenbosch / Remote
Placements24
Posted 9 days ago
Job Viewed
Job Description
About the Role
Our client, a forward-thinking biopharmaceutical company, is looking for an experienced Remote Pharmaceutical Clinical Trial Manager to lead and oversee clinical trials globally. This position is fully remote, offering the flexibility to work from anywhere within South Africa. The successful candidate will be responsible for the planning, execution, and completion of clinical trials in accordance with ICH-GCP guidelines, regulatory requirements, and company protocols. You will manage all aspects of trial conduct, including site selection, patient recruitment, data collection, and budget management. This role requires strong leadership skills, meticulous attention to detail, and a deep understanding of clinical trial operations. You will work closely with investigators, study coordinators, CROs, and internal cross-functional teams to ensure the successful and timely delivery of trial milestones. We are seeking a proactive and results-oriented professional who is passionate about advancing medical research and bringing innovative therapies to patients. This remote opportunity allows for a global impact while maintaining work-life balance.
Key Responsibilities- Develop comprehensive clinical trial protocols, study plans, and budgets.
- Oversee the selection, initiation, monitoring, and close-out of clinical trial sites.
- Ensure compliance with ICH-GCP guidelines, regulatory requirements, and company SOPs.
- Manage and mentor Clinical Research Associates (CRAs) and other study personnel.
- Act as the primary point of contact for investigators, site staff, and external vendors.
- Monitor trial progress, identify risks, and implement mitigation strategies to ensure timely completion.
- Oversee data management activities, ensuring data accuracy, completeness, and integrity.
- Manage clinical trial budgets and track expenditures.
- Prepare regulatory submission documents and respond to regulatory agency queries related to clinical trials.
- Collaborate with cross-functional teams, including medical affairs, R&D, and pharmacovigilance.
- A Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree or equivalent is preferred.
- A minimum of 5-7 years of experience in clinical trial management within the pharmaceutical or biotech industry.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in managing multi-center clinical trials, including global trials.
- Strong project management skills with the ability to manage timelines, budgets, and resources effectively.
- Excellent leadership, communication, and interpersonal skills.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Ability to work independently and collaboratively in a remote setting.
- Strong problem-solving and decision-making capabilities.
- Experience in specific therapeutic areas (e.g., oncology, cardiology) is a plus.
Our client offers a competitive salary, performance-based bonuses, and a comprehensive benefits package. This includes medical aid, retirement fund contributions, and generous paid time off. We provide substantial opportunities for professional development, including leadership training and participation in industry conferences. This position is fully remote, allowing you to work from your preferred location in South Africa. Our client is committed to fostering a supportive, collaborative, and inclusive virtual work environment. You will have the opportunity to work on innovative drug development programs and contribute significantly to global health. Join a dynamic team dedicated to advancing patient care through rigorous clinical research.
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6
Job Description
A leading automotive manufacturing company is seeking an experienced Analytical Chemist to join their Paintshop division in East London.
Key Responsibilities:
• Conduct qualitative and quantitative chemical analysis on production blends and materials
• Perform laboratory testing, method development, validation, and reporting
• Support quality control processes and ensure compliance with MBAG standards
• Operate, maintain, and calibrate laboratory equipment and analytical instruments
• Support continuous improvement initiatives and provide technical expertise to production and suppliers
• Participate in ISIR material evaluations and hazardous chemical assessments
Minimum Requirements:
• BSc Degree in Analytical Chemistry, Chemistry, or related scientific field (NQF 7)
• 3–5 years’ analytical laboratory experience in manufacturing, automotive, paint, or chemical environments
• Strong knowledge of analytical instruments, laboratory methods, and quality systems
• Experience with QMS, ISIR, and automotive paint/coating standards advantageous
• Strong analytical, reporting, and problem-solving skills
• Advanced MS Office proficiency
• Willingness to work weekends when required for production support
Suitable candidates are invited to submit their CVs to:
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7
Job Description
About the Role Our client, a dynamic pharmaceutical company with a growing presence in South Africa, is actively seeking a highly organized and experienced Clinical Trials Manager to oversee clinical research operations in George, Western Cape . This critical role will involve managing all aspects of clinical trials, from site initiation to study close-out, ensuring adherence to ethical standards, regulatory requirements, and company protocols. You will be responsible for managing budgets, timelines, and resources to ensure the successful execution of clinical development programs. The successful candidate will possess strong leadership skills and a deep understanding of Good Clinical Practice (GCP) guidelines. This is a fantastic opportunity to make a significant impact on the development of new pharmaceutical products that improve patient outcomes. The role requires your full presence at our George facilities to ensure direct oversight and efficient management of all trial activities. Key Responsibilities
- Develop and implement comprehensive clinical trial protocols and management plans.
- Select, train, and monitor clinical investigators and site staff to ensure compliance with protocols and GCP.
- Manage trial budgets, track expenses, and ensure timely delivery of project milestones.
- Oversee the collection, data management, and quality assurance of trial information.
- Liaise with regulatory authorities, ethics committees, and other relevant stakeholders.
- Identify and mitigate risks associated with clinical trial execution.
- Prepare clinical study reports and contribute to regulatory submissions.
- Foster strong relationships with clinical sites and external partners.
- Ensure all trial activities are conducted ethically and in accordance with international standards.
- Bachelor's degree in a life science, nursing, or related field; Master's degree or equivalent experience preferred.
- Minimum of 7 years of experience in clinical trial management within the pharmaceutical industry or a Contract Research Organization (CRO).
- In-depth knowledge of ICH-GCP guidelines, clinical trial methodologies, and regulatory requirements in South Africa and internationally.
- Proven experience in managing multiple clinical trials simultaneously.
- Excellent leadership, communication, and interpersonal skills.
- Strong organizational and project management abilities, with meticulous attention to detail.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Ability to travel as required for site visits and meetings.
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8