Clinical Research Associate, Pharma Trials | Travel & Benefits

Placements24

Kempton Park

On-site

ZAR 480,000 - 720,000

Full time

5 days ago
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Benefits offered by this job

Health benefits
Dental & vision benefits
Company car or travel allowance
Paid time off
Career advancement

Job summary

Placements24 in South Africa seeks a detail-oriented Clinical Research Associate to support pharmaceutical trials from their Tembisa operations. You will monitor sites to ensure protocol adherence, regulatory compliance, and data integrity, acting as the main liaison between sponsor and investigators.

The role requires a life sciences degree with 3+ years of CRA experience, strong knowledge of GCP/ICH, and experience with EDC and CTMS systems.

Qualifications

  • Bachelor's degree in life sciences; advanced degree preferred.
  • Minimum 3 years of CRA experience in pharmaceutical industry.
  • In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
  • Experience with EDC systems and CTMS.
  • Excellent organizational skills and ability to manage multiple priorities.
  • Strong written and verbal communication skills.

Responsibilities

  • Conduct site initiation, interim monitoring, and close-out visits per protocol and GCP guidelines.
  • Verify the accuracy, completeness, and integrity of clinical data at study sites.
  • Ensure regulatory compliance with protocols and regulations at all sites.
  • Serve as primary contact between sponsor and investigative sites.
  • Train site staff on study procedures and documentation requirements.
  • Generate monitoring reports following each site visit.

Skills

Attention to detail
Organizational skills
Verbal communication
Written communication

Education

Bachelor's degree in life sciences
Advanced degree preferred

Tools

EDC systems
CTMS

Job description

Placements24 in South Africa seeks a detail-oriented Clinical Research Associate to support pharmaceutical trials from their Tembisa operations. You will monitor sites to ensure protocol adherence, regulatory compliance, and data integrity, acting as the main liaison between sponsor and investigators.

The role requires a life sciences degree with 3+ years of CRA experience, strong knowledge of GCP/ICH, and experience with EDC and CTMS systems.

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