Senior Clinical Research Associate- CNS - (Mid Atlantic)
About The Position
Worldwide Clinical Trials is hiring a Senior Clinical Research Associate (CRA) to manage investigative-site activities and support high-quality, compliant clinical trial delivery. The role spans the study lifecycle, from site identification and start-up through maintenance and close-out, and involves close partnership with investigative sites, sponsors, and study teams. Psychiatry experience is required to help guide sites, support effective data collection, and protect patient safety. This is a home-based role supporting sites in the Mid-Atlantic territory. Candidates must reside within the territory to support site visits and study activities. The role involves travel to investigative sites approximately 8–10 days per month, primarily regionally, with occasional travel elsewhere as needed. The posting also refers to seeking candidates based in the Southeast. The Clinical Operations environment offers regular coaching conversations and professional development support, with a potential career path toward 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 Mid-Atlantic territory to support site visits and study activities.
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 study lifecycle, from site identification and start-up through study maintenance and close-out.
- Coordinate study start-up, including collecting required regulatory documentation and supporting contract and budget negotiations.
- Conduct Study Initiation Visits (SIVs) 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.
- Professional development support.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
