Join our Talent Pool - Sr Clinical Research Associate ( Croatia)

📋 Description

• Independently conduct and document onsite and remote monitoring activities, including site
• Ensure investigative sites comply with study protocols, ICH-GCP, applicable local regulations, SOPs
• Serve as a primary point of contact for assigned sites, managing site-related questions, issues
• Review clinical trial data, source documentation and study systems to ensure accuracy
• Support site selection, activation and recruitment activities, working with sites to achieve study
• Ensure sites are appropriately trained on protocols, study systems, processes and applicable

🎯 Requirements

• Bachelor's degree (Honours) in Life Sciences, Health Sciences, Pharmacy, Nursing or a related
• 4–6 years of relevant clinical research experience, with 7–9 years preferred.
• Strong clinical site monitoring experience across clinical trial activities from site start-up
• Thorough knowledge of ICH-GCP, clinical research principles and applicable local regulatory
• Experience with Phase I–IV clinical trials preferred.
• Proficiency with clinical trial systems such as EDC, IRT, eTMF, CTMS and Microsoft Office, with

🎁 Benefits

• Education Reimbursement program for full-time employees
• Monthly Cell Phone and Remote Work Allowance (dependent on role eligibility)
• One time office setup allowance (can be used to purchase a scanner/printer, extra monitor, office
• Working while visiting program – up to 4 weeks per year!
• Flexible Summer Hours Program from May – September
• Employee referral incentive – we know great people know other great people, and we think that