Clinical Research Associate 2
Hybrid · Bucharest, București, Romania
Job Summary
Design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments. Conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance, data integrity, and patient safety. Collaborate with investigators and site staff to facilitate study conduct, perform data review and resolve queries to maintain high-quality data, and contribute to the preparation and review of study documentation including protocols and clinical study reports. Requires a bachelor's degree in a scientific or healthcare-related field, at least 2 years of CRA experience, knowledge of ICH-GCP guidelines, strong organizational and communication skills, ability to work independently and collaboratively, and willingness to travel ~60% with an on-site presence in Bucharest 2–3 times per week when not monitoring. The role is based in Romania with travel as needed and will involve working from the Bucharest office with sponsor ICON, a global healthcare research organization. Inclusion and accessibility commitments are noted, with reasonable accommodations available during recruitment.
Required Qualifications
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills, with attention to detail
- Ability to work independently and collaboratively in a fast-paced environment
- Willingness to travel as required (approximately 60%)
- Available to work from the client’s Bucharest office 2–3 times per week when not conducting monitoring visits
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