Contractor Clinical Research Associate (CRA)

About the role

The Contractor Clinical Research Associate (CRA) will manage clinical study sites from selection through close‑out, ensuring data quality, regulatory compliance, and timely execution in line with Tigermed and sponsor SOPs, ICH‑GCP and local regulations.

Key responsibilities

• Identify and qualify study sites, conduct pre‑study visits and site initiation visits (SIV).
• Perform routine monitoring visits, source‑data verification (SDV), and issue resolution.
• Provide ongoing GCP and protocol training to site staff.
• Maintain essential study documentation, manage trial master files and archiving.
• Coordinate safety reporting, including timely SAE submission.
• Finalize site budgets, secure contracts, and oversee payment schedules.
• Update and maintain study tools and systems throughout the project.

Required profile

• Bachelor’s degree or higher in Medicine, Pharmacology, Biology or related field.
• Minimum 1 year of experience as a CRA.
• Strong knowledge of Good Clinical Practice (GCP) and clinical trial processes.

Required skills

• Proficiency with Microsoft Word.
• Proficiency with Microsoft Excel.

What we offer

• Opportunity to work on diverse clinical studies with an international sponsor.
• Flexible contract arrangement.