Senior CRA - Remote with East Coast Travel

Worldwide Clinical Trials; Florida; Remote; USD 97.000 - 193.000; Vollzeit

Zusammenfassung

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to support East Coast sites from a home-based position. You will lead site qualification, monitoring, and data quality efforts across multiple studies, traveling approximately 8–10 days per month.

The ideal candidate has 5+ years as a regional CRA, with experience in psychiatric trials and strong regulatory knowledge. This role emphasizes high-quality study delivery and proactive site partnership.

Qualifikationen

• Bachelor's Degree or a Nursing Degree and 5+ years as a regional, traveling CRA.
• Experience monitoring psychiatric clinical trials is required.
• Travel within the specified region; 8–10 days per month.
• Full-service monitoring experience is preferred.
• Strong knowledge of clinical trial processes, site management, and regulatory requirements.

Aufgaben

• Manage clinical research activities at investigative sites participating in Worldwide studies.
• Identify and assess potential research sites to support study execution.
• Coordinate start-up activities, including regulatory documentation and support for contracts/budgets.
• Conduct Pre-Site, Study Initiation, Interim Monitoring, and Closeout visits.
• Train site personnel on protocol requirements, data collection, and safety reporting.
• Monitor site performance and provide ongoing support throughout study maintenance.
• Ensure informed consent, safety reporting, and regulatory compliance.
• Partner with sites and teams to drive data quality and participant safety.
• Support site closeout activities and ensure study requirements are completed at closeout.

Kenntnisse

Site monitoring

Regulatory compliance

Clinical trial management

Team collaboration

Ausbildung

Bachelor's Degree or Nursing Degree

Jobbeschreibung

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to support East Coast sites from a home-based position. You will lead site qualification, monitoring, and data quality efforts across multiple studies, traveling approximately 8–10 days per month.

The ideal candidate has 5+ years as a regional CRA, with experience in psychiatric trials and strong regulatory knowledge. This role emphasizes high-quality study delivery and proactive site partnership.