Cardiovascular CRA II – Hybrid

Placements24

Cape Town

Hybrid

ZAR 540,000 - 860,000

Full time

5 days ago
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Benefits offered by this job

Health insurance
Dental and Vision insurance
Retirement plan
Paid time off

Job summary

Placements24 is seeking a diligent Clinical Research Associate II (CRA II) for a hybrid role in Cape Town, Western Cape. You will monitor trial sites to ensure data integrity, patient safety, and protocol compliance, with travel 40–60%.

The ideal candidate has a life-science degree, 3+ years as a CRA, and experience in cardiovascular trials, using EDC/CTMS systems, and strong communication skills.

Qualifications

  • Bachelor’s degree in a life science, nursing, or related field; Master’s degree a plus.
  • Minimum 3 years as a CRA or equivalent in pharma/biotech.
  • Experience monitoring clinical trials, preferably cardiovascular.

Responsibilities

  • Conduct site initiation, routine monitoring, and close-out visits.
  • Verify data via source data verification.
  • Ensure adherence to GCP, protocols, and regulatory requirements.
  • Manage data queries promptly and communicate findings.
  • Build relationships with investigators and sites; communicate with sponsors.
  • Prepare monitoring visit reports with findings and actions.
  • Identify site-specific issues and risks to patient safety and data quality.
  • Facilitate regulatory audits and sponsor inspections as needed.
  • Contribute to study documents and training site staff.

Skills

CRA monitoring
Regulatory compliance
Data integrity
Site communication
EDC systems
CTMS
Travel readiness
Team player

Education

Bachelor’s degree in life science/nursing/related field
Master’s degree (a plus)

Tools

EDC
CTMS

Job description

Placements24 is seeking a diligent Clinical Research Associate II (CRA II) for a hybrid role in Cape Town, Western Cape. You will monitor trial sites to ensure data integrity, patient safety, and protocol compliance, with travel 40–60%.

The ideal candidate has a life-science degree, 3+ years as a CRA, and experience in cardiovascular trials, using EDC/CTMS systems, and strong communication skills.

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