Senior Clinical Research Associate- CNS -Psychiatry - East Coast
About The Position
Worldwide Clinical Trials is hiring a home-based Senior Clinical Research Associate to support clinical research sites across the East Coast, with a focus on CNS and psychiatry studies. The role manages site activities throughout the clinical study lifecycle, from site identification and start-up through study maintenance and closeout, with an emphasis on quality, patient safety, and regulatory compliance. The associate collaborates with investigative sites, sponsors, and global study teams and travels to sites approximately 8–10 days per month, primarily regionally, with occasional travel elsewhere as needed. The role includes support for regulatory submissions, trial master file management, and site management, as well as regular coaching and development conversations with a Line Manager. The position offers a potential career path to Clinical Trial Manager opportunities.
Requirements
- Bachelor’s degree from a four-year university or a Nursing Degree.
- At least 5 years of experience as a Clinical Research Associate.
- Experience in Psychiatry.
- Excellent interpersonal, oral, and written communication skills, including proficiency in English.
- Strong organizational skills, excellent attention to detail, and the ability to work with little or no supervision.
- Proficiency in Microsoft Office, CTMS, and EDC systems.
- Residence on the East Coast and willingness to travel regionally.
Nice To Haves
- Experience in full-service monitoring.
Responsibilities
- Manage research activities at investigative sites participating in Worldwide clinical research projects.
- Support sites throughout the clinical study lifecycle, from identification and start-up through maintenance and closeout.
- Coordinate study start-up activities, including collecting appropriate regulatory documents and supporting contract and budget negotiations.
- Conduct study initiation visits and train sites on accurate data collection and safety event reporting.
- Monitor site activities and help ensure compliance with informed consent, safety reporting, and applicable regulatory requirements.
- Partner with sites and study teams to address site management needs and support successful study delivery.
Benefits
- Competitive benefits package depending on location.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
