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CRA position to be filled:

Location: Cape Town, Durban and Johannesburg

Link to apply for the position is below:

Purpose of the position:

The CRA is responsible for conducting project activities associated with the monitoring functions of Phase I-IV clinical studies while continuing to develop his/her knowledge of the drug development process, Good Clinical Practices, and relevant regulations.

The CRA manages investigator site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines, study documents (including protocol and plans) and Standard Operating Procedures (SOPs).

The CRA is the first point of contact for investigators and site staff and will maintain regular contact with study site to ensure GCP/ICH/Protocol compliance, assessment of subject accrual rates and respond to internal team requests.

The CRA is involved in the coordination, support and documentation of projects throughout all stages of the development process, with particular focus on the clinical phases. As a CRA, S/he will report to the GARDP CTM at project level and be responsible for monitoring and keeping track of GARDP resources for given projects.


· Fully remote , Cape Town, Johannesburg or Durban based

To apply

· Please submit your application using the online form

· Deadline for application: Accepting applications until 16 February 2022

Drugs for Neglected Diseases initiative (DNDi) &

Global Antibiotic R&D Partnership (GARDP)

P.O Box 333 / Muizenberg / 7950 / South Africa.


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