Senior Clinical Research Associate - CNS(US, Midwest)
Worldwide Clinical Trials
Worldwide Clinical Trials seeks a Senior Clinical Research Associate to manage research activities at clinical trial sites, primarily in a remote capacity with regional travel. The role involves site selection, study initiation, regulatory compliance, and ongoing site management across CNS and rare disease programs.
Responsibilities
- Oversee all stages of clinical studies at participating research sites from initiation through closure
- Conduct study initiation visits and ensure regulatory document collection and contract negotiation
- Train sites on data collection procedures and safety event reporting protocols
- Monitor site compliance with informed consent and regulatory requirements throughout studies
- Manage ongoing site activities remotely with periodic in-person oversight visits
Requirements
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree or nursing degree
- Expertise in CNS/Neurology and Rare Disease therapeutic areas
- Proficiency with Microsoft Office, CTMS, and EDC systems
- Excellent English communication skills, both written and oral
- Current residence in the Midwest region
- Willingness to travel regionally
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