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Careers in South Africa
DEVELOP YOUR CAREER WITH PPD
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| Clinical Contracts Specialist |
You will be the primary contact for investigative sites for contractual issues and negotiations, and be responsible for all activities required to finalise Statement of Agreements (SOA)/Site contracts and financial agreements with investigative sites, pharmacies, laboratories or other relevant contractual parties. You will be required to review SOA/contract templates to ensure compliance with local legislation and practices and develop or adapt SOA/contract templates to meet client demands (where required).
The successful candidate will possess excellent organisational, communication and problem solving skills. You will also be proficient in Word, Excel, Outlook, and database use. Candidates must be able to work on their own initiative as well as in a team, and have the ability to work with people at all levels.
You will have an LLB or B. Proc degree and will either be part way through your articles, or recently qualified. Previous experience within a contract research organisation or pharmaceutical company would be desirable, but not essential.
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| Clinical Research Associate/Senior Clinical Research Associate |
You will be primarily tasked to set up and monitor clinical trials
conducted in South Africa as part of international projects. You should thrive
in multi-national project teams and be focused on delivering exemplary
levels of customer service.
With a life sciences degree or nursing
qualification and at least one years experience of Phase II-IV
trials, you will have in depth knowledge of FDA and ICH GCP
requirements.
SCRAs will have a minimum of two years experience, including experience of start-up, monitoring and close-out. As a SCRA you will have the opportunity to mentor more junior CRAs and may be asked to take on project coordination activities as a lead CRA.
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| Research Assistant/Project Assistant |
As a research assistant or project assistant you will provide vital support for clinical research projects. You will have excellent communication and organisational skills and a self-motivated, flexible and professional attitude. You must be able to prioritise and work well within a multi-national team environment and have an in-depth knowledge of Microsoft Word, Excel and preferably PowerPoint.
Project assistants will have a good standard of education and two years administration experience.
Research assistants will have a life science/nursing qualification and at least six months administration experience. The research assistant role will provide the training required to progress and become a clinical research associate. |
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| Clinical Contracts Specialist |
You will be the primary contact for investigative sites for contractual issues and negotiations, and be responsible for all activities required to finalise Statement of Agreements (SOA)/Site contracts and financial agreements with investigative sites, pharmacies, laboratories or other relevant contractual parties. You will be required to review SOA/contract templates to ensure compliance with local legislation and practices and develop or adapt SOA/contract templates to meet client demands (where required).
The successful candidate will possess excellent organisational, communication and problem solving skills. You will also be proficient in Word, Excel, Outlook, and database use. Candidates must be able to work on their own initiative as well as in a team, and have the ability to work with people at all levels.
You will have an LLB or B. Proc degree and will either be part way through your articles, or recently qualified. Previous experience within a contract research organisation or pharmaceutical company would be desirable, but not essential.
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