Senior CRA, Psychiatry – Remote & Travel

Worldwide Clinical Trials Holdings, Inc.; Texas; Hybride; USD 97 000 - 193 000; Plein temps

Résumé du poste

Worldwide Clinical Trials Holdings, Inc. is seeking a Senior Clinical Research Associate for a home-based role supporting sites across the Central United States.

You will monitor studies, ensure protocol adherence, and coordinate regulatory documentation with global teams. The ideal candidate has 5+ years as a regional traveling CRA and experience in CNS/psychiatric trials, with the ability to travel 8–10 days per month.

Qualifications

• Bachelor's Degree or Nursing Degree required.
• 5+ years as a regional traveling CRA.
• Experience monitoring CNS and psychiatric trials.
• Willingness to travel regionally; 8–10 days per month.
• Experience in full-service monitoring preferred.
• Strong knowledge of clinical trial processes, site management, regulatory requirements.

Responsabilités

• Manage clinical research activities at investigative sites participating in Worldwide studies.
• Identify and assess potential research sites to support study execution.
• Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes.
• Conduct monitoring visits: PSSVs, SIVs, IMVs and COVs.
• Train site personnel on protocol requirements, data collection processes, and safety reporting expectations.
• Monitor site performance and provide ongoing support throughout study maintenance activities.
• Ensure compliance with informed consent requirements, safety reporting obligations, and regulatory standards.
• Partner with sites and study teams to drive data quality, participant safety, and overall study success.

Connaissances

Site management

Clinical trials

Travel coordination

Formation

Bachelor's degree

Nursing degree

Description du poste

Worldwide Clinical Trials Holdings, Inc. is seeking a Senior Clinical Research Associate for a home-based role supporting sites across the Central United States.

You will monitor studies, ensure protocol adherence, and coordinate regulatory documentation with global teams. The ideal candidate has 5+ years as a regional traveling CRA and experience in CNS/psychiatric trials, with the ability to travel 8–10 days per month.