O pozici
We are seeking a Freelance Site Feasibility Specialist to support the successful identification and selection of investigator sites across Europe. This role is highly operational and site-facing, focusing on feasibility outreach, data collection, and tracking, while ensuring high standards of communication, organization, and confidentiality. You will work closely with internal study teams and external sites to gather key information that supports efficient study start-up and site selection.
Co budeš dělat
- Conduct site-facing outreach to investigators and study sites across Europe
- Distribute feasibility questionnaires and follow up to ensure timely responses
- Act as a key point of contact for feasibility-related communication
- Support the collection of feasibility data (SSQ, site information, etc.)
- Track responses and maintain accurate records in internal systems
- Ensure timely reporting of feasibility status to stakeholders
- Assist with data entry and monitoring of feasibility responses
- Coordinate and support the collection of Confidentiality Disclosure Agreements (CDAs)
- Ensure proper tracking and documentation of all agreements
- Maintain compliance with internal processes and timelines
- Maintain clear and professional communication with sites and internal teams
- Collaborate with study start-up, site identification, and project teams
- Provide regular updates on feasibility progress and any challenges
Koho hledáme
- Experience in: Clinical research (CRO, pharma, biotech)
- Minimum of 2-3 years in site feasibility, site ID, or study start-up
- Strong organizational and tracking skills
- Excellent communication skills (written and verbal)
- Experience working with: Feasibility questionnaires (SSQ) and CDA collection processes
- Ability to manage multiple sites and timelines simultaneously
- Fluent in English (additional European languages are a plus)
