Wits Solutions Careers – Study Coordinator

Website Wits Health Consortium

Job Description:

To administer, maintain and coordinate the logistical aspects of clinical trials according to good clinical practice, the study protocol and the standard operating procedures and to act as a pivotal point of contact for the clinical trial team and the donors.

Job Responsibilities:

  • Ensure completion of corrective action of internal and external QC reports and monitoring reviews  Assist with staff training (and retraining) where error trends are identified
  • Prepare files for monitoring visits and requirements.
  • Meet with Monitors as and when required.
  • Take ownership and accountability for tasks and demonstrate effective self-management.
  • Follow through to ensure that quality and productivity standards of own work are consistently and accurately maintained.

Job Requirements:

  • Display a concern for patients and willingness to respond to patients’ needs and requirements
  • Able to prioritise own workload, take initiative (pro-active) and work to tight deadlines.
  • Ordered and systematic in approach to tasks, with strict to compliance to protocolsAble to exercise discretion and independent decision-making.
  • Thorough with good attention to detail.
  • Good communication skills.

Qualification & Experience:

  • Proficiency in MS office.
  • Relevant tertiary qualification.
  • A valid driver’s license.
  • Minimum 2-3 years clinical trial experience

Job Details:

Company: Wits Health Consortium

Vacancy Type: Full Time

Job Functions: N/A

Job Location: Hillbrow, Gauteng, SA

Application Deadline: N/A

Apply Here


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