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All you need to know about the ethical conduct of health research in humans in one course! Covering USA, EU and SA regulations, guidelines, principles, key standards and norms as well as the ethical considerations, role, responsibilities and reporting requirements from ethics committees when conducting health research. We also discuss the sensitive issues around fraud and misconduct and uncover conflict of interest as well as ethical tensions and dilemmas when conducting research with placebos, human biological materials, enrolling intensive care and terminal care patients and a look at ethics in genetic research. -
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 date is 16 October 10h00 – 16h00.
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If you work in the clinical research industry, it’s crucial that you stay up to date with the latest regulations and guidelines and be compliant. If you need to renew your GCP compliance training, then our immersive and engaging online refresher course is perfect for you. The course covers both ICH GCP and SA GCP guidelines, can be completed in 4 hours, and fulfils the criteria of the TransCelerate mutual recognition program. Enrol now and take the first steps on your career journey -
The pharmaceutical and clinical research industries tend to work in silos, and staff in support roles are typically only involved in a specific section of the clinical trial life cycle. It's time to break these silos and help staff in support roles see the bigger picture, so that they understand where they fit in the clinical research puzzle, the value of their roles, and how they contribute to participant safety, data integrity, and the overall success of a trial. Having a good overview and broad understanding of the clinical research journey will improve the communication between silos, as well as the confidence, performance, and adaptability of staff in support roles across the clinical trial industry. This course was specifically designed by industry experts, and can be completed in 3 hours. This course does not confer GCP-compliance.
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