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Senior Clinical Data Associate - South Africa - FSP

Parexel · Algeria, Angola, Benin, Botswana, British Indian Ocean Territory, Burkina Faso, Burundi, Cabo Verde, Cameroon, Central African Republic, Chad, Comoros, Congo, Congo, The Democratic Republic of the, Côte d'Ivoire, Djibouti, Egypt, Equatorial Guinea, Eritrea, Eswatini, Ethiopia, French Southern Territories, Gabon, Gambia, Ghana, Guinea, Guinea-Bissau, Kenya, Lesotho, Liberia, Libya, Madagascar, Malawi, Mali, Mauritania, Mauritius, Mayotte, Morocco, Mozambique, Namibia, Niger, Nigeria, Rwanda, Réunion, Saint Helena, Ascension and Tristan da Cunha, Sao Tome and Principe, Senegal, Seychelles, Sierra Leone, Somalia, South Africa, South Sudan, Sudan, Tanzania, Togo, Tunisia, Uganda, Western Sahara, Zambia, Zimbabwe

Clinical Research
Remote
Not yet analysed
Demand79
Career growth74
Healthcare fit72
Remote potential92
5-year outlook
Clinical data management demand is generally stable, with progression toward clinical data manager or study lead roles; pay will vary by South Africa market, sponsor, and prior data-management experience, so exact figures should not be assumed from the posting.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
full-time
Date found
2026-10-28

Intelligence details

Flexible work details

Engagement type
Permanent
Hours
Full-time
Rate period
Annual

Listing via Himalayas.

Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.

Why this is worth applying to

Worth applying if you have clinical trial coordination, data review, or EDC/GCP exposure and want a remote clinical-research operations path. Clinicians without data-management experience may find the senior title a stretch.

Who should apply

Research nurses, clinical trial coordinators, pharmacists or doctors with GCP/EDC exposure, and healthcare graduates with CRO or clinical data review experience, particularly those based in South Africa.

CV angle

Reframe real clinical work as protocol-driven data collection, source documentation, adverse-event reporting, query resolution, and cross-functional collaboration; quantify study volumes, data accuracy, timelines, and compliance where genuine.

Skills to highlight

  • Clinical data management
  • Electronic Data Capture (EDC)
  • eCRF design/review
  • Query management
  • SAE reconciliation
  • ICH-GCP
  • Database lock
  • CRO/vendor oversight

Role summary

Remote clinical data management role supporting Phase I-IV trials: reviewing protocols and eCRFs, coordinating EDC systems, managing queries and reconciliations, maintaining data management plans, and supporting database lock with CRAs, statisticians, programmers, and vendors.

We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.