Remote Clinical Trial Manager - Lead Multi-Site Trials

Placements24

Rustenburg

Hybrid

ZAR 900,000 - 1,300,000

Full time

6 days ago
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Benefits offered by this job

Medical aid
Bonus structure
Retirement fund contribution
Professional development

Job summary

Placements24 is seeking a Remote Clinical Trial Manager to oversee planning, execution, and completion of complex trials from a remote South Africa setting. You will lead cross-functional teams, ensure adherence to GCP and regulatory guidelines, and drive study timelines across multiple therapeutic areas.

The ideal candidate has 5+ years in trial management, extensive CTMS/EDC experience, and a track record of managing multi-center studies while working independently in a fully remote

Qualifications

  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
  • Minimum of 5 years of clinical trial management experience in pharma or CRO.
  • Proven ability to manage multi-center trials across therapeutic areas.
  • Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
  • Excellent leadership and remote team management skills.
  • Proficiency with CTMS and EDC systems.

Responsibilities

  • Develop and manage trial protocols, budgets, and timelines.
  • Oversee site and staff selection, training, and performance management.
  • Ensure compliance with GCP, ICH, and local regulations.
  • Mentor CRAs and other study personnel.
  • Coordinate with data management, biostatistics, and regulatory affairs.
  • Monitor trial progress and implement mitigation strategies.
  • Prepare study progress reports for senior management.

Skills

Leadership
Remote work
Project management
Communication

Education

Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field
Master's degree preferred

Tools

CTMS
EDC

Job description

Placements24 is seeking a Remote Clinical Trial Manager to oversee planning, execution, and completion of complex trials from a remote South Africa setting. You will lead cross-functional teams, ensure adherence to GCP and regulatory guidelines, and drive study timelines across multiple therapeutic areas.

The ideal candidate has 5+ years in trial management, extensive CTMS/EDC experience, and a track record of managing multi-center studies while working independently in a fully remote

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