Freelance Clinical Research Associate

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

We have various freelance, part-time, remote vacancies of Clinical Research Associate (CRA) for studies we are running throughout Europe and CIS.

Location: EU or CIS regions.

• 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, assist in agreements
• Provide monitoring visits and site management

• University degree in Life Science field
• 2-5 year’s experience as CRA (independent monitoring)
• In depth therapeutic and protocol knowledge
• Deep knowledge in 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

• Professional growth and career opportunities
• Supportive work environment
• International team

Biomapas is a functional and full outsourcing solution provider to the global life science industry. As a trusted partner for biopharmaceutical and medical device companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory, pharmacovigilance and medical information excellence across Europe, CIS, EAEU, MENA, LATAM regions and the US throughout the entire product lifecycle.

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