Associate Clinical Research Associate
Merck · Bucuresti (ana Tower), Romania
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Merck seeks a Clinical Research Associate to serve as primary site contact and manager for clinical trial sites. The role involves study oversight, site monitoring, regulatory compliance, and cross-functional coordination to ensure high-quality trial execution across all study phases.
What they're looking for
- Associate degree in scientific/healthcare field plus 3 years relevant healthcare experience, or equivalent
- Fluent in Romanian and English, written and verbal communication
- Knowledge of ICH-GCP standards, clinical research phases, and country-specific regulations
- Proficiency with MS Office and clinical trial management systems
- Strong documentation practices and quality compliance mindset
- Ability to travel domestically and internationally 65-75% of working time
What you'll be doing
- Serve as primary site contact and manager for assigned clinical trial sites throughout study lifecycle
- Conduct remote and on-site monitoring activities to ensure data quality, accuracy, and subject safety
- Perform site visits including initiation, monitoring, validation, and close-out activities
- Manage regulatory documentation and maintain accurate study records in clinical trial management systems
- Identify and resolve site performance, compliance, and quality issues with escalation as needed
Privacy & handoff
This role links to Merck's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.