Senior CRA - Remote, Travel-Friendly CNS/Alzheimer's Trials

Worldwide Clinical Trials; Missouri; A distancia; USD 97.000 - 193.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Senior CRA to lead monitoring and site management for CNS and Alzheimer's trials. This home-based role supports sites across the Central United States, with travel approximately 8–10 days per month.

The ideal candidate has a Bachelor’s or Nursing degree and 5+ years as a regional traveling CRA, with full-service monitoring experience preferred. You’ll partner with sites and study teams to ensure protocol adherence, safety, and data quality.

Formación

• Bachelor's Degree or Nursing Degree required.
• 5+ years as a regional, traveling Clinical Research Associate.
• Experience monitoring CNS and Alzheimer's trials.
• Requires travel within the specified region; 8–10 days per month.

Responsabilidades

• Manage clinical research activities at investigative sites participating in Worldwide trials.
• Identify and assess potential research sites to support study execution.
• Coordinate study start-up activities including collection of regulatory documentation and budget/contracts.
• Conduct monitoring visits: PSSVs, SIVs, IMVs, COVs.
• Train site personnel on protocol requirements, data collection and safety reporting.
• Monitor site performance and provide ongoing support throughout maintenance activities.
• Ensure informed consent, safety reporting and regulatory compliance.

Conocimientos

Traveling CRA experience

Site management

Educación

Bachelor's Degree

Nursing Degree

Descripción del empleo

Worldwide Clinical Trials is seeking a Senior CRA to lead monitoring and site management for CNS and Alzheimer's trials. This home-based role supports sites across the Central United States, with travel approximately 8–10 days per month.

The ideal candidate has a Bachelor’s or Nursing degree and 5+ years as a regional traveling CRA, with full-service monitoring experience preferred. You’ll partner with sites and study teams to ensure protocol adherence, safety, and data quality.