14 Clinical Lead jobs in South Africa
Clinical Lead
Posted today
Job Viewed
Job Description
About the Company
Founded in 2017, Medi2data powers access to consented and curated medical data through cutting-edge technology and specialist services. We streamline and digitise the secure exchange of medical information, supporting GP practices, Instructing parties, and patients. By addressing challenges on both the demand (Client Services) and supply (Primary Care Services) sides of the ecosystem, we enable faster, more efficient, and compliant medical data transactions. We are transforming how medical data is accessed and managed in the digital age.
This role operates across Medi2data's three core divisions - Primary Care Services, Client Services, and Medi2cert - delivering innovative, technology-driven solutions to GP practices, enterprise clients, and consumers. Our Primary Care Services division supports GP practices in streamlining medical reporting through eMR, our SaaS platform, and eMR+, our fully managed outsourced service - ensuring accuracy, security, and efficiency in producing electronic GDPR compliant medical reports. Client Services works with enterprise clients to facilitate the fast, compliant, and secure delivery of medical evidence, leveraging AI-driven automation, digital workflows, and clinical expertise to enhance decision-making and operational efficiency. Medi2cert (D2C) provides consumers with seamless access to premium medical certification services, allowing them to obtain the documentation they need quickly and securely.
Across all three divisions, we combine advanced technology, clinical governance, and a customer-centric approach to deliver market-leading solutions. As an NHS-accredited supplier, we uphold the highest standards of data security and compliance, ensuring that our partners and customers can confidently rely on the integrity and efficiency of our services. This role is integral to driving innovation and operational excellence across the Medi2data Group.
The Role
Reports To
: Head of Operations
Banding:
Band 3
Location & Term
: Cape Town; Full-time (Monday – Friday); Permanent; On-site
Job Overview:
The Clinical Lead will be an experienced, GMC-registered medical doctor with a strong background in clinical governance, quality assurance, and patient safety. They will be responsible for upholding and continuously improving the highest standards of clinical quality, governance, and safety across Medi2data's medical reporting services.
This role combines medical expertise with strategic and operational leadership. The Clinical Lead will support and guide both the clinical and operational teams to ensure that all medical reporting activities are carried out with accuracy, integrity, and efficiency. They will serve as the senior clinical authority within the business, providing oversight on complex or escalated cases, resolving clinical issues and complaints, and ensuring that lessons learned translate into measurable improvements.
In addition, the Clinical Lead will take ownership of clinical communication within the organisation, ensuring alignment and clarity between clinical and non-clinical teams. Externally, they will represent Medi2data in all clinical matters, engaging with clients, regulators, and stakeholders to build trust and maintain the organisation's reputation for excellence.
The position requires a proactive leader who can balance clinical rigour with operational pragmatism, driving innovation in processes while safeguarding quality and patient safety at all times.
Key Responsibilities:
Clinical Leadership & Governance
- Lead on clinical quality assurance and auditing of medical reports.
- Develop and embed Medi2data's clinical governance framework, working collaboratively with the Clinical Governance & Safety Officer.
- Ensure compliance with professional, ethical, and regulatory standards in all clinical activities.
- Monitor clinical risks and contribute to incident reviews, learning, and continuous improvement initiatives.
- Take ownership of handling clinical issues and complaints, ensuring prompt investigation, resolution, and learning from outcomes.
Medical Reporting & Review
- Undertake review and preparation of medical reports and certificates.
- Review and validate complex or escalated medical reports to support the medical reporting nurses.
- Provide clinical advice and guidance to clinicians and operational colleagues on case queries.
- Ensure consistency, clarity, and accuracy in clinical reporting.
Team Collaboration & Development
- Work closely with the Clinical Operations Manager to maintain smooth clinical workflows.
- Act as a mentor and clinical point of escalation for the Medical Reporting Nurses.
- Contribute to training, professional development, and feedback within the clinical team.
- Promote collaboration across departments and levels of the organisation, ensuring clinical and business success.
- Foster a culture of clinical excellence, patient safety, and evidence-based practice.
Clinical Communication & Representation
- Serve as the primary point of contact for internal communication on clinical matters, ensuring clarity and alignment across teams.
- Represent Medi2data in external clinical communications, engaging with stakeholders, clients, and regulators as required.
- Prepare and deliver updates, reports, and briefings on clinical issues to internal leadership and external partners.
Strategy & Continuous Improvement
- Support the design and implementation of clinical policies, procedures, and best practices.
- Drive innovation in clinical processes, ensuring efficiency without compromising quality.
- Stay up-to-date with relevant clinical guidelines and regulatory developments, advising the business on implications.
Clinical Lead
Posted today
Job Viewed
Job Description
Marie Stopes South Africa with a footprint in Gauteng, Kwazulu-Natal, the Western Cape and Eastern Cape is part of the MSI Reproductive Choices Group, recognised as one of the world's leading providers of sexual and reproductive healthcare with over 9,000 team members working in 37 countries across the world.
We know that access to reproductive choice is life changing, accordingly we focus on sustainable delivery, efficiency, and funding models that are built to last, so that the women and girls we serve today will have a choice in the future too.
MSI Reproductive Choices is committed to creating an inclusive environment with a workforce which is representative of the communities we serve. We're proud to be an equal opportunities employer and give equal consideration to all qualified applicants without regard to race, ethnicity, religion, gender, gender identity or expression, sexual orientation, national origin, disability, or age. We are committed to promoting equality and safeguarding the welfare of all team members and clients, with a focus on vulnerable groups.
ABOUT THE ROLE
The Regional Clinical Lead will provide 1st and 2nd trimester surgical termination of pregnancy services and the applicable family planning methods across all centres in Gauteng. Responding to clinical client queries, providing guidance on the interpretation of laboratory results. Working closely with the Clinical Director and the Clinical Governance Team on the implementation of applicable MSI and MSSA Clinical Guidelines and Policies.
QUALIFICATIONS AND EXPERIENCE
The following requirements are a prerequisite to be considered for the position:
- You are Pro-Choice
- MBChB essential
- Experienced Gynecologist/Obstetrics Medical Doctor
- Preferred experience in the provision of TOP services
- Registered with the HPCSA
- Competency in Ultrasound advantageous
LOCATION
Gauteng
Job Type: Permanent
Work Location: In person
Clinical Lead Physiotherapist
Posted today
Job Viewed
Job Description
Director of Health and Social Care - South Ayrshire Partnership - Elgin House
Permanent: 35 hours
Location: Ailsa Hospital
Salary: £143,702
FOR FURTHER INFORMATION ON THIS POSITION AND TO APPLY PLEASE USE THE BELOW LINK:
Director of Health and Social Care - South Ayrshire Partnership - Elgin House - SOA11009 | South Ayrshire Council | myjobscotland
Clinical and Coaching Lead
Posted 24 days ago
Job Viewed
Job Description
About Our Client
Our client is a pioneering digital health organisation committed to expanding access to high-quality, patient-centred care across sub-Saharan Africa. By combining clinical expertise, health coaching, and cutting-edge technology, they deliver solutions that tackle chronic diseases, women's health, and mental wellness. With a mission-driven culture, strong growth trajectory, and focus on impact, the organisation offers a unique opportunity to transform healthcare outcomes at scale.
The Role: Clinical and Coaching Lead
As the Clinical and Coaching Lead, you will spearhead clinical strategy, operational excellence, and education programs. You will guide multidisciplinary teams, implement evidence-based practices, and leverage digital and AI-driven tools to deliver innovative, scalable, and effective health solutions.
Key Responsibilities
Oversee and optimise clinical operations to ensure efficient, high-quality, patient-centred services
Lead, mentor, and inspire multi-disciplinary clinical and coaching teams for collaboration and performance
Develop and implement clinical protocols, quality standards, and best practices
Design and execute health coaching and education programs focusing on chronic disease, women's wellness, and mental health
Collaborate with technology and data teams to integrate AI-driven tools into care delivery and personalised coaching
Establish, monitor, and evaluate program metrics to measure effectiveness, outcomes, and patient engagement
Represent the organisation at conferences, forums, and with key stakeholders
Contribute clinical expertise to strategic planning and business development initiatives
About You
Medical degree (MBBS or equivalent) or advanced qualification in Nursing, Public Health, Clinical Psychology, or related field
8 to 10 years of healthcare experience, with at least 5 years in leadership roles
Expertise in chronic disease management, reproductive/maternal health, or mental health
Proven success in leading multi-disciplinary teams and implementing evidence-based initiatives
Familiarity with AI, digital health tools, and data-driven healthcare strategies
Exceptional communication, presentation, and stakeholder engagement skills
Innovative, agile, and adaptable in dynamic, fast-paced environments
Willingness to travel for partnerships, conferences, and stakeholder engagement
Senior Clinical Data Science Lead
Posted today
Job Viewed
Job Description
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.
Senior Clinical Data Science Lead (Advanced Clinical Data Manager)
Sponsor Dedicated
South Africa
We are currently seeking a Senior Clinical Data Science Lead to join our diverse and dynamic team. As a Senior Clinical Data Science Lead at ICON, you will play a pivotal role in leading the analysis, interpretation, and management of clinical data to drive the success of our clinical trials. You will contribute to the advancement of innovative treatments and therapies by overseeing data science initiatives and ensuring data quality and integrity across studies.
What You Will Be Doing
- Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, and reporting.
- Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs.
- Overseeing the analysis of clinical data to provide actionable insights that inform study decisions and outcomes.
- Providing strategic guidance on data governance, quality control, and compliance with regulatory requirements.
- Establishing partnerships with key stakeholders to leverage the latest advancements in data science and technology in clinical research.
Your Profile
- Advanced degree in a relevant field such as data science, biostatistics, or life sciences.
- Extensive experience in clinical data science, with a strong focus on data management and analysis in clinical trials.
- Strong leadership skills and a proven ability to manage cross-functional teams in a fast-paced, matrix environment.
- Expertise in data analysis tools, statistical software, and data visualization techniques.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive change in a complex organization.
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
Interested 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
Senior Clinical Data Science Lead
Posted today
Job Viewed
Job Description
Senior Clinical Data Science Lead (Sponsor Dedicated)
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
Senior Clinical Data Science Lead (Advanced Clinical Data Manager)
Sponsor Dedicated
South Africa
We are currently seeking a Senior Clinical Data Science Lead to join our diverse and dynamic team. As a Senior Clinical Data Science Lead at ICON, you will play a pivotal role in leading the analysis, interpretation, and management of clinical data to drive the success of our clinical trials. You will contribute to the advancement of innovative treatments and therapies by overseeing data science initiatives and ensuring data quality and integrity across studies.
What You Will Be Doing:
- Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, and reporting.
- Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs.
- Overseeing the analysis of clinical data to provide actionable insights that inform study decisions and outcomes.
- Providing strategic guidance on data governance, quality control, and compliance with regulatory requirements.
- Establishing partnerships with key stakeholders to leverage the latest advancements in data science and technology in clinical research.
Your Profile:
- Advanced degree in a relevant field such as data science, biostatistics, or life sciences.
- Extensive experience in clinical data science, with a strong focus on data management and analysis in clinical trials.
- Strong leadership skills and a proven ability to manage cross-functional teams in a fast-paced, matrix environment.
- Expertise in data analysis tools, statistical software, and data visualization techniques.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive change in a complex organization.
LI-Remote
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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised 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
Interested 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.
Senior Clinical Data Science Lead (Sponsor Dedicated)
Posted 25 days ago
Job Viewed
Job Description
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.
**Senior Clinical Data Science Lead (Advanced Clinical Data Manager)**
**Sponsor Dedicated**
**South Africa**
Clinical Data Management Expertise. The CDM will perform scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS).
**What you will be doing:**
+ Tapping into your technical and clinical expertise, performing scientific data review with focus on complex indication and therapy related elements of the study
+ Involved in study related activities from the protocol design stage onwards, providing input into the study specific and/or indication specific data collection tools.
+ Close partnership with study physician(s) and study scientist(s) in order to establish, align and confirm scientific clinical data review expectations for assigned trial(s).
+ Reviews content and integration requirements for eCRF and other data collection tools
+ Reviews (complex) scientific study data, manages queries and holds discussions with relevant stakeholders. Involvement in other review activities (e.g., Coding, SAE reconciliation) is possible.
+ Leads and attends meetings as appropriate.
+ Establishes conventions and quality expectations for clinical data.
+ Works in collaboration with the study physicians, study scientists, global data managers, statisticians and other stakeholders
+ Identifies and communicates lessons learned and best practices.
**Qualifications**
+ Bachelor's degree or higher, preferably in a health/scientific discipline
+ 5+ years of Clinical Data Management experience
+ Robust experience with EDC (E.g. Medidata Rave) and use of Data Review tools such as J‐Review
+ Deep understanding of drug development
+ Strong technical skills, including experience working with using Microsoft Excel functionality
+ Excellent written and oral communication skills
**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 maximise savings and plan with confidence for the years ahead
+ Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: 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, colour, 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 through the form below.
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.
#LI-JC3
#LI-Remote
**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
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Clinical Data Management Lead, home-based in South Africa
Posted 10 days ago
Job Viewed
Job Description
+ Serve as primary point of contact for customer on data management deliverables
+ Manage multiple large studies or program of studies (possibly global)
+ Provide leadership and senior support to DTLs on multiple large global programs of global studies
+ Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise
+ Lead direct negotiations with customer, e.g., timelines, financial, process, resources
+ Meet with Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables
+ Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects
+ Serve as the escalation point for unresolved data issues
+ Ensure appropriate resources are assigned to meet project deliverables
+ Create and/or review and sign-off on all data management plan (DMP) documents
+ Manage service performance and provide leadership to identify root causes of issues and implement remedial actions
+ Serve as Subject Matter Expert (SME)
+ Provide leadership and expertise in a specific CDM task or technology
+ Independently manage SOW/budget
+ Independently bring process improvements and solutions to the CDM team/CDM department
+ Lead a focus team or global or local best practice team
+ Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
+ Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients)
+ Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation)
+ Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently
+ Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology
+ Knowledge of operating procedures and work instructions and the ability to apply them in practice
+ Knowledge of Good Clinical Practices and relevant regulatory guidelines
+ Excellent communication, interpersonal, customer service, and teamwork skills
+ Excellent organizational and problem-solving skills
+ Excellent project management skills
+ Ability to work independently
+ Comprehensive understanding of clinical drug development process
+ Ability to establish and maintain effective working relationships with co-workers, managers and customers
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
+ Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field
+ Around 7 years direct Data Management experience, including 5 or more years as a CDM project lead; or equivalent combination of education, training and experience
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 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
Clinical Data Management Lead, home-based in South Africa
Posted 10 days ago
Job Viewed
Job Description
+ Serve as primary point of contact for customer on data management deliverables
+ Manage multiple large studies or program of studies (possibly global)
+ Provide leadership and senior support to DTLs on multiple large global programs of global studies
+ Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise
+ Lead direct negotiations with customer, e.g., timelines, financial, process, resources
+ Meet with Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables
+ Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects
+ Serve as the escalation point for unresolved data issues
+ Ensure appropriate resources are assigned to meet project deliverables
+ Create and/or review and sign-off on all data management plan (DMP) documents
+ Manage service performance and provide leadership to identify root causes of issues and implement remedial actions
+ Serve as Subject Matter Expert (SME)
+ Provide leadership and expertise in a specific CDM task or technology
+ Independently manage SOW/budget
+ Independently bring process improvements and solutions to the CDM team/CDM department
+ Lead a focus team or global or local best practice team
+ Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
+ Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients)
+ Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation)
+ Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently
+ Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology
+ Knowledge of operating procedures and work instructions and the ability to apply them in practice
+ Knowledge of Good Clinical Practices and relevant regulatory guidelines
+ Excellent communication, interpersonal, customer service, and teamwork skills
+ Excellent organizational and problem-solving skills
+ Excellent project management skills
+ Ability to work independently
+ Comprehensive understanding of clinical drug development process
+ Ability to establish and maintain effective working relationships with co-workers, managers and customers
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
+ Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field
+ Around 7 years direct Data Management experience, including 5 or more years as a CDM project lead; or equivalent combination of education, training and experience
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 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
Clinical Data Management Lead, home-based in South Africa
Posted 10 days ago
Job Viewed
Job Description
+ Serve as primary point of contact for customer on data management deliverables
+ Manage multiple large studies or program of studies (possibly global)
+ Provide leadership and senior support to DTLs on multiple large global programs of global studies
+ Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise
+ Lead direct negotiations with customer, e.g., timelines, financial, process, resources
+ Meet with Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables
+ Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projects
+ Serve as the escalation point for unresolved data issues
+ Ensure appropriate resources are assigned to meet project deliverables
+ Create and/or review and sign-off on all data management plan (DMP) documents
+ Manage service performance and provide leadership to identify root causes of issues and implement remedial actions
+ Serve as Subject Matter Expert (SME)
+ Provide leadership and expertise in a specific CDM task or technology
+ Independently manage SOW/budget
+ Independently bring process improvements and solutions to the CDM team/CDM department
+ Lead a focus team or global or local best practice team
+ Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
+ Previous experience and proven competence in managing delivery of multiple global trials through full DM life-cycle (i.e. large trials of at least 1000 patients)
+ Demonstrated expert data management skills and advanced knowledge of the data management process (e.g., therapeutic area, extensive knowledge in DM processes, SAE reconciliation, external data vendor reconciliation)
+ Previous experience and proven competence in handling complex customer negotiations and bid defense meetings independently
+ Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology
+ Knowledge of operating procedures and work instructions and the ability to apply them in practice
+ Knowledge of Good Clinical Practices and relevant regulatory guidelines
+ Excellent communication, interpersonal, customer service, and teamwork skills
+ Excellent organizational and problem-solving skills
+ Excellent project management skills
+ Ability to work independently
+ Comprehensive understanding of clinical drug development process
+ Ability to establish and maintain effective working relationships with co-workers, managers and customers
**MINIMUM REQUIRED EDUCATION AND EXPERIENCE**
+ Bachelor's Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field
+ Around 7 years direct Data Management experience, including 5 or more years as a CDM project lead; or equivalent combination of education, training and experience
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 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