Job Summary
A company is looking for a Senior Project Coordinator in Poland.
Key Responsibilities
- Prepare and review essential clinical trial and regulatory documents for Investigator Sites
- Establish site activation timelines and coordinate activities to meet these timelines
- Communicate with clinical sites and collaborate with other departments to ensure alignment on site activation targets
Required Qualifications
- Bachelor's degree in a field relevant to clinical research or equivalent experience
- Minimum of 2 years of experience as a Project Coordinator or equivalent in clinical research
- Proven Site Start-Up experience in managing clinical trials in a global environment
- Good knowledge of essential documentation requirements for clinical trials
- Proficiency in English; bilingualism in French or another language is an asset
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