Worldwide Clinical Trials is a global contract research organization that supports pharmaceutical and biotechnology companies throughout the drug development lifecycle. With more than 30 years of experience, the company provides clinical monitoring, data management, patient recruitment, and regulatory consulting across therapeutic areas including oncology, cardiology, and rare diseases. Its approach combines broad clinical trial expertise with personalized support and tailored solutions for complex studies.
Senior Clinical Research Associate, Psychiatry
Monitor psychiatric and CNS trials at investigative sites across the Central United States. Support site startup, compliance, data quality, and study closeout at Worldwide Clinical Trials.
Description
- Oversee clinical research at sites participating in Worldwide studies.
- Evaluate potential research sites for study participation.
- Coordinate study startup, including regulatory documents and contract and budget processes.
- Conduct PSSVs, SIVs, IMVs, and COVs.
- Train site staff on protocols, data collection, and safety reporting.
- Track site performance and assist with ongoing study activities.
- Verify informed consent, safety reporting, and regulatory compliance.
- Work with sites and study teams to maintain data quality, participant safety, and study progress.
- Help sites complete closeout activities and remaining study requirements.
Requirements
- Bachelor’s or nursing degree.
- At least five years of experience as a regional or traveling Clinical Research Associate.
- Experience monitoring CNS and psychiatric clinical trials.
- Travel within the assigned region, with 8–10 days on site per month.
- Full-service monitoring experience preferred.
- Strong knowledge of clinical trial processes, site management, and regulatory requirements.
- Must reside within the Central United States territory.
Benefits
- Benefits package varies by location.
- Transparent compensation and pay equity.