Senior CRA — Home-Based, CNS Trials, Midwest Travel

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

Descripción de la vacante

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to lead site monitoring and ensure regulatory compliance across the Midwest region. This home-based role partners with investigative sites, study teams, and sponsors to drive data quality and patient safety.

You'll travel regionally (8–10 days per month), oversee start-up through closeout, mentor site staff, and uphold high standards in trial conduct and documentation.

Formación

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

Responsabilidades

• 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 and support contract/budget processes.
• Conduct monitoring visits: PSSVs, SIVs, IMVs, COVs.
• Train site personnel on protocol, data collection and safety reporting.
• Monitor site performance and provide ongoing study support.
• Ensure informed consent, safety reporting and regulatory compliance.
• Collaborate with sites and study teams to drive data quality and safety.
• Support site closeout activities and ensure study requirements are completed.

Conocimientos

Regional travel experience

CNS clinical trials experience

Site management knowledge

Regulatory knowledge

Full-service monitoring

Educación

Bachelor's Degree or Nursing Degree

Descripción del empleo

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to lead site monitoring and ensure regulatory compliance across the Midwest region. This home-based role partners with investigative sites, study teams, and sponsors to drive data quality and patient safety.

You'll travel regionally (8–10 days per month), oversee start-up through closeout, mentor site staff, and uphold high standards in trial conduct and documentation.