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Senior Clinical Research Associate, CNS (Arizona Remote)
Oversee CNS clinical trial sites for Worldwide Clinical Trials, from study start-up through closeout. Manage site compliance, maintenance, training, and safety reporting remotely.
Description
- Oversee research activities at sites participating in Worldwide Clinical Trials projects.
- Identify sites that may be suitable for research studies.
- Coordinate study start-up, including collection of site regulatory documents.
- Assist with contract and budget negotiations.
- Train site staff in proper data collection and reporting potential safety events.
- Manage site activities throughout study maintenance.
- Close out site research activities when studies end.
- Conduct study initiation visits (SIVs).
- Ensure sites meet informed consent, safety reporting, and applicable regulatory requirements.
Requirements
- Strong interpersonal, spoken, and written English communication skills.
- Excellent organization and attention to detail.
- Able to work with minimal supervision.
- Proficient with Microsoft Office, CTMS, and EDC systems.
- At least five years of Clinical Research Associate experience.
- Four-year university degree or nursing degree.
- CNS experience strongly preferred.
- Must reside on the West Coast.
- Available for regional travel.
Benefits
- Support with regulatory submissions and TMF management, plus in-house CRA support for projects requiring extensive site management.
- Regular check-ins and coaching with a Line Manager.
- Defined career development opportunities, including progression to Clinical Trial Manager roles.
- Access to the Executive Leadership team.
- Competitive benefits package that varies by location.
- Transparent compensation and commitment to pay equity.