Senior Clinical Research Associate – CNS/Oncology
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Job Description
Senior Clinical Research Associate managing UK CNS/Oncology clinical research sites for global CRO Worldwide Clinical Trials. Overseeing study start-up, site maintenance, safety reporting, and closeout.
Responsibilities:
- Manage research activities at sites participating in clinical research projects, predominantly registries and other non-interventional/observational studies
- Identify potential sites to participate in research
- Perform study start-up activities, including collecting regulatory documents from sites
- Support negotiation of contracts and budgets
- Train sites to collect data properly and report potential safety-related events
- Manage site activities during study maintenance
- Close down research activities at sites after study conclusion
- Conduct study initiation visits (SIVs)
- Perform remote site management while ensuring informed-consent compliance, safety-event reporting, and adherence to applicable regulatory requirements
Requirements:
- Excellent interpersonal, oral, and written communication skills in English
- Superior organizational skills with attention to detail
- Ability to work with little or no supervision
- Proficiency in Microsoft Office, CTMS, and EDC systems
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree or RN/BSN in Nursing
- Willingness to travel
- Strong CNS and Oncology experience required
- Hematology experience is a plus
Benefits:
- Diverse and inclusive work environment
- Supportive and cohesive teams
- Accessible, hands-on leadership
- Equal employment opportunities
- Employee opportunities to thrive and develop professionally
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