Remote Senior Clinical Trial Leader

Placements24

Gauteng

Remote

ZAR 1,200,000 - 1,800,000

Full time

14 days+
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Benefits offered by this job

Annual leave
Health insurance
Retirement planning
Employee Assistance Programme
Life assurance

Job summary

ICON Clinical Research in South Africa offers a Senior Clinical Trial Manager role focused on country-level delivery in a sponsor-dedicated model. You will lead local study teams, drive startup activities, and ensure regulatory submissions align with protocol requirements and ICH GCP.

You will manage budgets, timelines, risk mitigation, and QA across the study lifecycle, collaborating with global teams and investigators to deliver successful trials.

Qualifications

  • Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
  • Significant clinical research experience in CRA/Senior CRA/Study Management or related role.
  • Strong knowledge of ICH GCP and country-specific regulatory requirements.
  • Proven leadership of cross-functional teams and full study lifecycle management.
  • Willingness to travel approximately 25%.

Responsibilities

  • Lead and coordinate Local Study Teams to deliver studies on time and on budget.
  • Oversee country-level startup activities, site activation, and regulatory submissions.
  • Manage country study progress, identify risks, and implement mitigations.
  • Guide CRAs on protocol compliance, ICH GCP, and local regulations.
  • Maintain TMF/eTMF and ensure inspection readiness; collaborate globally.

Skills

Leadership
Project management
Cross-functional teams
Willingness to travel

Education

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related discipline

Job description

ICON Clinical Research in South Africa offers a Senior Clinical Trial Manager role focused on country-level delivery in a sponsor-dedicated model. You will lead local study teams, drive startup activities, and ensure regulatory submissions align with protocol requirements and ICH GCP.

You will manage budgets, timelines, risk mitigation, and QA across the study lifecycle, collaborating with global teams and investigators to deliver successful trials.

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