Senior Clinical Research Associate (CRA)

About the role

We are seeking an experienced Senior Clinical Research Associate to join our global, mid‑size CRO. Based in North Macedonia, you will lead on‑site monitoring activities and act as the primary liaison between study sites and internal teams, ensuring high‑quality data collection and regulatory compliance.

Key responsibilities

• Conduct and report Site Initiation Visits (SIV), Routine Monitoring Visits (RMV) and Close‑out Visits (COV) on‑site.
• Perform CRF review, source document verification and query resolution.
• Manage site communication, act as the main point of contact for vendors and in‑house support services.
• Collaborate with internal project teams to track study progress.
• Participate in feasibility research and support regulatory submissions.
• Prepare for and take part in audits and inspections.

Required profile

• University degree in Life Sciences or equivalent education/experience.
• Independent on‑site monitoring experience in Phase II and/or III trials.
• Full working proficiency in English and Macedonian.
• Valid driver’s license and ability to travel.

Required skills

• Proficiency with MS Office applications.

What we offer

• Opportunity to broaden therapeutic area expertise.
• Professional development in clinical research.
• Dynamic, supportive work environment within a global organization.