SrClinical Research Associate and Local Start-Up Specialist Contractor - Ukraine
RemoteUkraine
UkraineRemotePart TimeEntry LevelMedium
Part TimeEntry LevelMedium
Job Summary
Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits. Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements while proactively identifying and resolving site issues to maintain trial integrity. Build strong relationships with investigators as the primary point of contact, overseeing site activation processes and regulatory affairs to ensure smooth study execution. Travel throughout Ukraine as required for this contractor role.
Required Qualifications
- Experience leading monitoring activities in complex trials
- Ideally in oncology or rare disease
- Minimum of at least 5 years' experience
- Strong understanding of ICH-GCP and regulatory guidelines
- Clear and confident communicator in English and local language
- Comfortable working independently and managing priorities
- Willingness to travel, as required
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