Job Position : Clinical Trials & Regulatory Affairs Coordinator (CTRA)
Location : Ifakara and Dar es Salaam
Reports to : Manager Clinical Trials and Operational Research Unit
The Clinical Trials and Regulatory Affairs Coordinator is a self-motivated individual who will provide support to NEOVITA project. He/ she will oversee the Efficacy of newborn Vitamin A supplementation in improving child survival in Tanzania.
QUALIFICATIONS :
- Bachelor Degree (s) in Medicine and/ or Nursing; Master’s in Public Health is an added advantage
- Not less than 3 years’ experience in coordinating tightly regulated international clinical trials as well as large scale field trials that involve women and children in African setting
- Excellent written and oral communication, with fluency in English as a working language. Should have good knowledge of computer software applications such as Ms Word, Excel and the Internet.
- Ability to work under pressure and timely meeting deadline, ability to plan, develop and work both independently as part of the team.
HOW TO APPLY:
Interested candidates should submit an application letter, a copy of their CV and names and contact information (e-mail addresses and telephone numbers) of three references; Applications should be submitted to:-
The Human Resource Manager
P.O.Box 79810
Dar es Salaam
Or through e –mail : mdh@mdh-tz.org indicating clearly, in the application letter, the position applied for.
Deadline of Application is 30th Aug, 2012
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