Join our global team as a 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
  • Fluent English language
  • 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


Benefits of being a part of our team:

  • 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.


Leave us your resume. And let’s have a chat.

Click or drag files to this area to upload. You can upload up to 2 files.

Big Enough To Cover  All Your Needs. Small Enough To Care.

Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Regulatory Affairs


Medical Information