Remote Clinical Research Associate – Trials & Data

Placements24

Mtubatuba Local Municipality

Hybrid

ZAR 1,143,000 - 1,796,000

Full time

5 days ago
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Benefits offered by this job

Competitive salary
Medical, dental, and vision insurance
Travel allowance for essential visits
Remote work

Job summary

Placements24 is seeking a diligent Remote Clinical Research Associate (Pharma) to support the execution of clinical trials across therapeutic areas. You will monitor study sites, ensure adherence to ICH-GCP, and maintain data integrity while working fully remotely from your location.

You will communicate with investigators and study teams, coordinate CTMS/EDC activities, and contribute to high-quality data collection for regulatory submissions, with a competitive benefits package and

Qualifications

  • Bachelor's degree in life science or related field.
  • Minimum 3 years of CRA experience in pharma.
  • Thorough understanding of ICH-GCP and regulatory requirements.
  • Experience with EDC systems and CTMS.
  • Excellent organizational and communication skills; ability to work independently and remotely.

Responsibilities

  • Perform remote and occasional on-site monitoring visits to verify data and protocol compliance.
  • Manage investigational product accountability and storage at sites.
  • Oversee site activation, training, and ongoing support for investigators.
  • Ensure timely collection and review of essential documents and queries.
  • Prepare monitoring visit reports and maintain stakeholder communications.

Skills

Remote work
Monitoring
Regulatory compliance
Communication

Education

Bachelor's degree in life sciences

Tools

EDC
CTMS

Job description

Placements24 is seeking a diligent Remote Clinical Research Associate (Pharma) to support the execution of clinical trials across therapeutic areas. You will monitor study sites, ensure adherence to ICH-GCP, and maintain data integrity while working fully remotely from your location.

You will communicate with investigators and study teams, coordinate CTMS/EDC activities, and contribute to high-quality data collection for regulatory submissions, with a competitive benefits package and

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