Description
To assist in clinical drug trials and evaluate the safety and efficacy of novel treatment or diagnostic options respecting strict ethical and scientific standards.
Key Performance Areas (KPA’s) & Responsibilities include, but not limited to:
- Performing duties required by a sub-investigator or principal investigator on clinical trials
- Providing clinical care and support to trial participants
- Assisting with medical trial procedures
- Working with a multidisciplinary team that includes laboratory, pharmacy, administrative and clinical staff, as well as public health representatives
- Helping to manage and coordinate projects
- Ensuring that ethical, regulatory and other network-related trial requirements are adhered to
- Assisting with training of other staff
Ideal Requirements
- Relevant MBCHB
- Current HPCSA registration
- At least 2 - 3 years’ experience as a medical doctor
- Passion for, and preferably some experience in, the field of clinical research
- Good Clinical Practice certificate (preferable)
Key Personal Inherent Characteristics
- Confidentiality
- Excellent verbal and written communication skills
- Excellent inter-personal skills
- High attention to detail
- Excellent follow up skills
- Professionalism
- Accountability
- Efficient and effective under pressure
- Flexible and able to work at all TASK sites (Bellville, Brooklyn and Delft)
Details:
Location: Cape Town, Western Cape
Contract Type: 12 Month Fixed Term Contract- TASK reserves the right to withdraw this advertisement and not fill the above-mentioned vacancy at any stage during the recruitment process.- Meeting our employment equity goals will be acknowledged during the recruitment process._