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Strengthen Your Trial’s Foundation: Master Data Governance in Clinical Research In clinical trials, participant safety is non-negotiable—but the bedrock of that safety is reliable, well-governed data. According to ICH GCP E6 (R3), both Sponsors and Investigators share equal responsibility for ensuring data integrity across the entire trial lifecycle. Data governance isn't just compliance—it's the foundation for generating credible evidence on the safety and efficacy of treatments. Poor data management risks more than protocol deviations; it jeopardizes trial outcomes, regulatory approvals, and ultimately, patient trust. This course empowers your team to take ownership of data across collection, verification, review, correction, protection, and analysis—ensuring every step is secure, traceable, and compliant. From setting up robust data policies to managing access and oversight, your team will gain practical strategies to uphold the scientific and ethical standards that drive successful trials. Don’t let weak data governance undermine your trial. Enrol your team now and build a culture of data accountability from start to finish. -
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Bundle at a Glance: Read More About The Courses Included- Total duration: 15 hours
- Delivery: 100% online with self-paced INTERACTIVE course material, virtual facilitation, practical tools, tips and downloadable templates.
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Bundle at a Glance: Read More About The Courses Included- Ethics in Health Research - A Global Perspective (2025)
- Mastering Essential Records: Foundations & Filing
- Total duration: 17 hours
- Delivery: 100% online with self-paced INTERACTIVE course material, virtual facilitation, practical tools, tips and downloadable templates.
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Bundle at a Glance: Read More About The Courses Included- Total duration: 14 hours
- Delivery: 100% online with self-paced INTERACTIVE course material, virtual facilitation, practical tools, tips and downloadable templates.
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The NIH policy released 16 September 2016 requires training on the protections for human research participants in addition to GCP training. The NDoH Ethics Guideline (2024), Section 5.4, also stipulates that health research ethics training is additional to discipline- or profession-specific and GCP training for anyone who wants to undertake research with human participants, before conducting research, to ensure they have the appropriate knowledge, skills, expertise, competence, including discipline-appropriate scientific background and research ethics training to conduct studies involving human participants. This course will teach you all you need to know about the ethical conduct of health research in humans! Covering USA, EU and SA regulations (South African Ethics in Health Research Guidelines: Principles, Processes and Structures, NDoH 2024, 3rd Edition), ethics guidelines, research methodologies, expectations for Research Ethics Committees (RECs) and descriptions of the research ethics infrastructure and regulatory framework in South Africa, USA and EU, principles, key standards and norms as well as the ethical considerations, role, responsibilities and reporting requirements from ethics committees when conducting health research. How does the programme work?
- Part 1: Online, self-paced eLearning course material. Complete Part 1 of the course anytime, and at your own pace on any devise, from anywhere in the world. The only requirement is that you need to complete it before attempting Part 2 of the programme – a virtual, facilitated session.
- Part 2: Qualified Facilitator led virtual session. The live facilitated session is hosted on Zoom and will be held on a set date and time. TRA will host one or more virtual Ethics sessions per month. Everyone that completes Part 1 of the programme is eligible to book for, and attend, a scheduled session, which can be done through the learning platform. If you miss a scheduled virtual session, you will need to join the following session. The virtual Ethics session dates can be found here.
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If you are outside of South Africa this is your entry ticket to a professional career in clinical research. If you are working in South Africa click here to be re-directed to our SA version of the course. Kickstart your journey in clinical trials with our immersive internationally accredited foundation course, which covers Good Clinical Practice Guidelines (ICH GCP), as well as the clinical trial life cycle. The course has been designed by industry experts to ensure you learn exactly what you need to start and / or further your career in clinical trials. The Foundations and Beyond course is more than just compliance training as it takes you on a journey through the full life cycle of a mock Phase III trial. For more information you can click here to download our course brochure. Enrol now and take the first steps on your career journey -
Your entry ticket to a professional career in clinical research in South Africa. If you are working outside of South Africa click here to be re-directed to our International version of the course. Kickstart your journey in clinical trials with our immersive internationally accredited foundation course, which covers Good Clinical Practice Guidelines (ICH GCP and SA GCP), as well as the clinical trial life cycle. The course has been designed by industry experts to ensure you learn exactly what you need to start and / or further your career in clinical trials. The Foundations and Beyond course is more than just compliance training as it takes you on a journey through the full life cycle of a mock Phase III trial. For more information you can click here to download our course brochure. The South African Health Regulatory Authority, SAHPRA, requires a virtual facilitation session as part of first time Good Clinical Practice training. To be compliant TASK Research Academy’s training will consist of two parts. To obtain your first time GCP certification you will be required to complete both parts. How does the program work?- Part 1: Pre-workshop course material. This comprehensive foundational pre-workshop course is mandatory and will take about 8-10 hours to complete. This part of the training is online. You can do it anytime, and at your own pace on any devise, from anywhere in the world. The only requirement is that you need to complete it before your virtual workshop. This course will provide you with all the knowledge and tools you need to actively participate and engage in the follow up virtual workshop (part two) to complement and enhance your learning experience during the workshop.
- Part 2: Qualified Facilitator led virtual workshop. There will be a set date and time for one or more virtual workshops in one month. Everyone that completed the pre-workshop course material before that date can join the workshop. If you missed the workshop you will need to join the next workshop. The next workshop dates can be found here.
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Bundle at a Glance: Read More About The Courses Included
- Foundations and Beyond - the Clinical Research Journey course and workshop - RSA
- OR Foundations and Beyond - The Clinical Research Journey - INTERNATIONAL
- Data Governance in Clinical Research
- Total duration: 21 hours
- Delivery: 100% online with self-paced INTERACTIVE course material, virtual facilitation, practical tools, tips and downloadable templates.
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-41%
Bundle at a Glance: Read More About The Courses Included
- Foundations and Beyond - the Clinical Research Journey course and workshop
- Ethics in Health Research - A Global Perspective (2025)
- Total duration: 26 hours
- Delivery: 100% online with self-paced INTERACTIVE course material, virtual facilitation, practical tools, tips and downloadable templates.
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-43%
Bundle at a Glance: Read More About The Courses Included
- Foundations and Beyond - the Clinical Research Journey course and workshop RSA
- OR Foundations and Beyond - The Clinical Research Journey - INTERNATIONAL
- Data Governance in Clinical Research
- Total duration: 23 hours
- Delivery: 100% online with self-paced INTERACTIVE course material, virtual facilitation, practical tools, tips and downloadable templates.
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-35%
Bundle at a Glance: Read More About The Courses Included
- Foundations and Beyond - the Clinical Research Journey course and workshop RSA
- OR Foundations and Beyond - The Clinical Research Journey - INTERNATIONAL
- Data Governance in Clinical Research
- Total duration: 20 hours
- Delivery: 100% online with self-paced INTERACTIVE course material, virtual facilitation, practical tools, tips and downloadable templates.
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-23%
Bundle at a Glance: Read More About The Courses Included- Total duration: 10 hours
- Delivery: 100% online with self-paced INTERACTIVE course material, practical tools, tips and downloadable templates.
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