Clinical Research Physician

Key roles and responsibilities of a Clinical Research Physician are:

Once trained, acting as principal investigator (PI) or sub-investigator ensuring ICH/GCP, and local regulations are met when conducting studies
Conducting clinical studies in line with the protocol and to ensure the recruitment of eligible participants
Review screening, pre-screening and screening success rates for clinical study delivery
Providing information and support to consenting participants for a clinical study
Responsible for checking participant inclusion/exclusion to studies
Collaborating closely with and developing positive relations with sponsors, clients and clients’ contractors as required, projecting a conducive and courteous company image
Carrying out clinical evaluation and clinical investigation of participants, ensuring protocol compliance, participant safety and quality data delivery
Constantly seeking and suggesting quality improvements
Taking ownership for ensuring serious adverse events / adverse events are reported appropriately

To be considered for this exciting opportunity you will need the following skills and experience:

Medical degree (MBChB or equivalent)
Registration with the Health Professions Council of SA (HPCSA)
Ideally, previous experience within clinical research
Have solid understanding of GCP (ICH/GCP and local regulations compliance, SA GCP)
Valid medical malpractice insurance
Demonstrate the inclination to provide practical help and mentorship to colleagues, providing practical solutions for any problems and supporting team development
Show meticulous attention to detail in recording participant information and data, ensuring queries are acted upon in a timely and efficient manner to deliver quality of the highest standard
Be a standout colleague, capable of building and sustaining positive relationships with colleagues, clients as well as study participants
Fluency in local SA languages advantageous