Clinical Research Associate (CRA) Lithuania

Join our global team as a Clinical Research Associate (CRA).

Clinical Research Associate (CRA) is responsible for coordinating and overseeing the execution of studies and clinical trials at investigational sites.

Position is in Lithuania.

Responsibilities:

• Study site monitoring and management (site selection, initiation, monitoring and close-out visits)
• Perform feasibilities and support start-up phase
• Create and maintain required study documentation (site management, monitoring, etc.)
• Ensure that clinical trials are conducted according to requirements (protocol, ICH-GCP, etc.)
• Administer protocol and related study training to assigned sites
• Perform regulatory document review and submission to regulatory authorities
• Prepare clinical trial documents and store, archive correspondence
• Negotiate study budgets with potential investigators/sites, assit in agreements
• Provide monitoring visits and site management

Requirements:

• University degree in Life Science field
• Fluent English language
• At least 1 year in clinical research field
• Experience as a CRA (independent monitoring) beneficial
• In depth therapeutic and protocol knowledge
• Deep knowledge of local regulations and clinical research regulatory requirements (GCP and ICH)
• Excellent skills in MS Office, EDC and other clinical trial related systems and platforms
• Attention to detail and time-management skills

Benefits of being a part of our team:

• Professional growth and career opportunities
• Supportive work environment
• Additional benefits (bonus system, additional health insurance and etc.)
• International team
• Modern and a new office in Kaunas with partly remote work possibility

 

Job Category: Clinical Research
Job Type: Full Time
Job Location: Lithuania
Job Specification: R2

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