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Clinical Research Associate; CRA; Pharmaceutical Trials

Remote / Online - Candidates ideally in
Cape Town, 7561, South Africa
Listing for: Placements24
Remote/Work from Home position
Listed on 2026-10-04
Job specializations:
  • Healthcare
    Clinical Research
Job Description & How to Apply Below
Position: Clinical Research Associate (CRA) - Pharmaceutical Trials
About the Role

Our client seeks a diligent and detail-oriented Clinical Research Associate (CRA) to oversee and manage clinical trials within the pharmaceutical sector in Cape Town . This role is crucial for ensuring the smooth and compliant execution of studies, directly contributing to the development of new life-saving medications. You will be responsible for site selection, monitoring, and close-out activities, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements.

This hybrid position offers the opportunity to combine remote work flexibility with essential on-site visits, making it ideal for a professional who values both autonomy and direct engagement in critical research oversight activities within a leading pharmaceutical company.

Key Responsibilities
  • Conduct site visits (initiation, monitoring, and close-out) to ensure compliance with protocols and regulations.
  • Verify the accuracy, completeness, and consistency of clinical data and source documentation.
  • Manage communication between investigators, study sites, and the internal study team.
  • Ensure adherence to Good Clinical Practice (GCP) and all applicable regulatory guidelines.
  • Identify and report any deviations, adverse events, or protocol violations promptly.
  • Maintain accurate and up-to-date study documentation and regulatory files.
Requirements
  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
  • Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
  • Thorough understanding of clinical trial processes , ICH guidelines, and GCP.
  • Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
  • Excellent communication, organizational, and time management skills.
  • Ability to travel to study sites as required (estimated 40-60% travel).
Benefits
  • Competitive annual salary commensurate with experience.
  • Comprehensive medical and retirement benefits package.
  • Generous travel allowance and expense reimbursement.
  • Professional development opportunities and continued education support.
  • A flexible hybrid work model supporting work-life balance.
Position Requirements
10+ Years work experience
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