Sr Clinical Research Associate (Serbia)

Alimentiv · Belgrade

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Role summary

Alimentiv seeks a Senior Clinical Research Associate for its Belgrade office to independently manage clinical trial monitoring and site oversight across Serbia and Croatia. This individual contributor role involves site qualification, protocol compliance, data integrity oversight, and mentoring junior staff in a gastrointestinal-focused CRO environment.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Lever, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-06 (originally posted 2026-10-06). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Bachelor's degree in Life Sciences, Health Sciences, Pharmacy, Nursing or related field
4–6 years clinical research experience, 7–9 years preferred
Strong site monitoring expertise from initiation through close-out
Proficiency with ICH-GCP, clinical research principles and local regulations
Experience with EDC, IRT, eTMF, CTMS and Microsoft Office platforms
Phase I–IV clinical trial experience preferred
Site management knowledge including activation, recruitment and training

What you'll be doing

Conduct onsite and remote monitoring activities, site qualification, initiation and close-out visits across Serbia and Croatia
Ensure investigative sites comply with protocols, ICH-GCP, regulations and study requirements
Serve as primary contact for assigned sites, resolving questions, issues and protocol deviations
Review clinical data, source documentation and systems for accuracy and data integrity
Support site selection, activation and patient recruitment milestone achievement

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