Remote Senior CRA – Oncology Trials & Global Impact

Placements24

Polokwane

Hybrid

ZAR 482,000 - 1,033,000

Full time

5 days ago
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Benefits offered by this job

Flexible remote work
Competitive hourly rate or project‑bas
Global team exposure
Professional development opportunities

Job summary

Placements24 seeks a Senior Clinical Research Associate to remotely monitor oncology trials, ensuring adherence to protocols, GCP, and regulatory requirements. This role supports sites worldwide from a home office, with emphasis on rigorous SDV and data integrity.

You will train site staff, manage relationships, prepare monitoring reports, and coordinate with internal teams and vendors. A life-science degree and 5+ years of CRA experience, especially in oncology, are required.

Qualifications

  • Bachelor's degree in life science, nursing, or related field; advanced degree preferred.
  • Minimum of 5 years as a CRA with oncology focus.
  • Strong knowledge of ICH GCP, regulations, and monitoring processes.

Responsibilities

  • Perform remote monitoring of trial sites to ensure protocol compliance and data integrity.
  • Oversee SDV via remote review of EHRs and study documents.
  • Build and maintain site relationships; train investigators and staff.
  • Identify issues and implement CAPAs to ensure trial quality.
  • Maintain regulatory documentation and drug accountability at sites.
  • Coordinate site initiation, interim monitoring, and site close-out remotely.
  • Prepare monitoring reports and participate in investigator meetings.
  • Act as a primary contact for sites and internal/external teams.

Skills

Remote monitoring
EDC systems
Oncology trials
ICH GCP knowledge
Time management
Communication

Education

Bachelor's degree in life science
Advanced degree preferred

Job description

Placements24 seeks a Senior Clinical Research Associate to remotely monitor oncology trials, ensuring adherence to protocols, GCP, and regulatory requirements. This role supports sites worldwide from a home office, with emphasis on rigorous SDV and data integrity.

You will train site staff, manage relationships, prepare monitoring reports, and coordinate with internal teams and vendors. A life-science degree and 5+ years of CRA experience, especially in oncology, are required.

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