Senior Clinical Research Associate - CNS/Psychiatry - West Coast - Remote
About The Position
We are a global, midsize Contract Research Organization (CRO) that is committed to innovation and pioneering creative approaches to find cures for persistent diseases. Our mission is to work with passion and purpose every day to improve lives. We are looking for individuals who share this pursuit and value making a difference for patients and their caregivers. At Worldwide Clinical Trials, we foster a diverse and inclusive environment that promotes collaboration and creativity, where people can thrive and do their best work. Our Clinical Operations team plays a crucial role in advancing clinical research, working alongside brilliant minds across various therapeutic areas. We offer extensive support through regulatory submissions, TMF management, and in-house CRAs. Professional development is a priority, with regular touchpoints and coaching, a clear career path, and opportunities to advance to Clinical Trial Manager roles. Our accessible Executive Leadership team is dedicated to advancing science and overcoming obstacles to improve patient lives.
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 Nursing Degree.
- Experience in CNS/Neurology is required.
- Psychiatry experience is strongly preferred.
- Candidates must reside on the West Coast.
- Willingness to travel regionally is required.
Responsibilities
- Managing the research activities at sites participating in clinical research projects.
- Involved in all stages of the clinical study, including identifying potential sites, performing study start-up activities (collecting regulatory documents, supporting contract and budget negotiation), training sites on data collection and safety reporting, managing site activities during study maintenance, and closing down research activities at sites.
- Conduct study initiation visits (SIVs).
- Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements, with most site management efforts performed remotely.
Benefits
- Competitive benefits package depending on location.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
