Clinical Research Associate – Senior CRA

• Prepare, conduct, and report on all types of monitoring visits, including site selection, initiation, routine monitoring, and close-out visits
• Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements
• Build and maintain strong relationships with investigators and site staff
• Monitor patient recruitment, study timelines, and site performance
• Perform source data verification, follow up on data queries, and manage site-level risks
• Oversee investigational product accountability, trial supplies, and essential study documentation
• Maintain Investigator Site Files (ISF) and support Trial Master File (TMF) reconciliation
• Deliver study-specific training to investigators and site staff
• Support regulatory submissions, audit preparation, and resolution of audit findings
• Collaborate with experienced clinical research professionals across different therapeutic indications

• MD, PharmD or MSc
• 1+ year of independent on-site monitoring experience in Ukraine
• Experience in all types of monitoring visits in Phase II and/or III
• Experience in Oncology/Ulcerative Colitis/Antibiotics trials is a plus
• Full working proficiency in English and Ukrainian
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel

• Remote work in Ukraine
• Opportunity to further develop skills
• Opportunity to widen therapeutic area experience
• Opportunity to become an expert in clinical research