Remote Senior CRA — Impactful Clinical Trials

Placements24

Gauteng

Remote

ZAR 650,000 - 900,000

Full time

3 days ago
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Benefits offered by this job

Health insurance
Dental insurance
Vision insurance
Retirement savings plan with matching
Generous paid time off
Travel allowance
Certifications support
Professional development opportunities

Job summary

Placements24 is seeking a Senior Clinical Research Associate (CRA) to join a remote team. The ideal candidate will monitor clinical trial sites, ensure data integrity, and uphold GCP and regulatory standards across trials.

This role requires strong organizational and communication skills and the ability to travel 50–60% to sites as needed. You will be a key liaison between site personnel and internal teams, contributing to successful trial execution within the Pharmaceutical industry.

Qualifications

  • Bachelor's degree in life sciences or related field.
  • 5+ years of CRA experience.
  • Strong knowledge of GCP/ICH guidelines and regulatory requirements.
  • Experience monitoring trials across therapeutic areas.
  • Proven ability to work remotely with minimal supervision.

Responsibilities

  • Conduct site initiation, interim monitoring, and close-out visits to ensure study compliance.
  • Verify data accuracy and source documents.
  • Ensure adherence to protocols and SOPs.
  • Manage relationships with investigators and site staff; provide training and support.
  • Monitor patient safety and report adverse events as required.

Skills

Site monitoring
GCP & ICH knowledge
Data integrity
Communication
Remote workload management

Education

Bachelor's degree in life sciences or related field

Tools

EDC systems
CTMS

Job description

Placements24 is seeking a Senior Clinical Research Associate (CRA) to join a remote team. The ideal candidate will monitor clinical trial sites, ensure data integrity, and uphold GCP and regulatory standards across trials.

This role requires strong organizational and communication skills and the ability to travel 50–60% to sites as needed. You will be a key liaison between site personnel and internal teams, contributing to successful trial execution within the Pharmaceutical industry.

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