Senior Clinical Research Associate – CNS/Oncology
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Job Description
Senior Clinical Research Associate managing CNS/Oncology clinical studies for Worldwide Clinical Trials, a global CRO. Overseeing site start-up, maintenance, compliance, and study closeout across the UK.
Responsibilities:
- Manage research activities at sites participating in clinical research projects, predominantly registries and non-interventional/observational studies
- Support all stages of clinical studies, including identifying potential sites
- Perform study start-up activities, including collecting regulatory documents
- Support negotiation of contracts and budgets
- Train sites on proper data collection and reporting potential safety-related events
- Manage site activities during study maintenance
- Close down research activities at sites after study conclusion
- Conduct study initiation visits (SIVs)
- Ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements while managing sites remotely
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, cohesive teams
- Accessible, hands-on leadership
- Professional growth and development opportunities
- Equal employment opportunities
- Exceptional employee experiences
- Remote work arrangement
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