The Botswana Medicines Regulatory Authority (BoMRA) is an organisation set up under the Medicines and Related Substances Act (MRSA) of 2013 and was established by the Botswana Government to regulate the supply chain of medicines and related substances, cosmetics and medical devices in order to ensure their quality, safety and efficacy. The Authority is looking for Talent to occupy the following position and become a part of a vibrant High performing team.
PROJECT OFFICER – Botswana Clinical Trials Regulation Project (XI)
WE ARE STILL MAKING CVs FOR P100. COVER LETTERS FOR P50
Pay with FNB EWallet to 76981238 or Orange Money on number 76981238
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Reporting to the Director- Pharmacovigilance & Clinical Trials Main Purpose of Job
The purpose of this role entails planning, organizing, and directing the completion of the BoCTRe project sponsored by European and Developing Countries Clinical Trials Partnerships, by ensuring the project work packages are completed on time, on budget, and within scope. You will be employed on a full-time basis for a period of 24 months.
Main Duties:
- You will analyze the current regulatory procedures for clinical trials in Botswana and identify gaps to be addressed and also assist in developing and implementing standardized SOPs, guidelines, and training programs for Institutional Review Board members. You will facilitate and participate in the conduct of training for the personnel involved in conduct of clinical research to follow the SOPs and guidelines.
- You will also participate in conducting of
Good Clinical Practice (GCP) inspections at different clinical research sites and work with IT department in the development and implementation of technological platform for submission and review of Clinical Trials (CT) protocols.
- Facilitate Steering Committee and provide logistics for training, travel, procurement, provide publicity for the project through relevant social media platforms and grant administrative support.
Qualifications
You will need to have degree in health sciences with 3 years’ experience in working in the area of conduct of clinical trials.
Competencies
The key competencies for the role include understanding of ICH – GCP guidelines, ethical conduct of clinical trials, clinical trial regulations- national and international. Proficiency in project management operating procedures, oversight and monitoring is desirable.
More Information
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JOB APPLICATION DETAILS
APPLICATION DETAILS
If you have the above capabilities kindly send your application, detailed CV and certified copies of certificates and national Id to [email protected]
Please ensure that you specify the job title in the subject of the email
NB: The Authority will only respond to the shortlisted
Closing date: 9th December 2021
Please say that you got this job advertisement through Jobs Botswana
- This job has expired!
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