Senior Clinical Research Associate-- CNS/ - Psychiatry - Southeast
About The Position
Worldwide Clinical Trials is seeking a home-based Senior Clinical Research Associate to support clinical research sites across the Southeast, with a focus on Psychiatry. The role manages site activities throughout the study lifecycle, from site identification and start-up through maintenance and close-out, helping ensure high-quality, compliant trial delivery and patient safety. The position collaborates with investigative sites, sponsors, and global study teams and includes approximately 8–10 days of travel per month, primarily within the region, with occasional travel elsewhere. Candidates must reside within the Southeast territory. The role is part of a collaborative Clinical Operations environment that offers regular coaching conversations and professional development support. The career path may lead to Clinical Trial Manager opportunities.
Requirements
- Four-year university degree or Nursing Degree.
- At least 5 years of experience as a Clinical Research Associate.
- Experience in Psychiatry.
- Excellent interpersonal, organizational, and communication skills, with strong attention to detail.
- Ability to work effectively with little or no supervision.
- Proficiency in Microsoft Office, CTMS, and EDC systems.
- Proficiency in English, including strong oral and written communication skills.
- Must reside within the Southeast territory.
Nice To Haves
- Experience in full-service monitoring.
Responsibilities
- Manage research activities at investigative sites participating in clinical research projects.
- Support sites throughout the study lifecycle, from site identification and start-up through maintenance and close-out.
- Coordinate study start-up activities, including collecting regulatory documentation and supporting contract and budget negotiations.
- Conduct Study Initiation Visits and train sites on accurate data collection and safety-event reporting.
- Manage ongoing site activities, primarily remotely, while maintaining effective communication and oversight.
- Ensure sites comply with informed consent requirements, safety reporting expectations, and applicable regulatory requirements.
- Partner with site teams to support high-quality study conduct and successful clinical trial delivery.
Benefits
- Competitive benefits package, depending on location.
- Regular coaching conversations and professional development support.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
