Senior CRA: Site Champion Driving Trial Success

Parexel; Chesapeake (VA); Vor Ort; USD 90.000 - 130.000; Vollzeit

Zusammenfassung

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to lead site management and monitoring for assigned investigator sites, ensuring patient safety and data quality in line with GCP, SMP, and sponsor standards.

The Sr. CRA will manage site relationships, enrollment and database release, and will collaborate with the Site Care Partner and study team to resolve protocol-related issues and optimize site performance throughout setup, conduct, and close-out.

Qualifikationen

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations.
• Experience in monitoring roles within clinical trials is required.
• Strong ability to interpret study protocols and regulatory requirements.

Aufgaben

• Ensure proper conduct of clinical trials in accordance with SMP, GCP and Sponsor standards.
• Manage operational aspects from site activation to database lock to meet timelines and quality.
• Serve as primary contact for investigator sites and coordinate with SCP for site delivery quality.

Kenntnisse

Clinical trial monitoring

ICH/GCP

FDA regulations

Jobbeschreibung

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to lead site management and monitoring for assigned investigator sites, ensuring patient safety and data quality in line with GCP, SMP, and sponsor standards.

The Sr. CRA will manage site relationships, enrollment and database release, and will collaborate with the Site Care Partner and study team to resolve protocol-related issues and optimize site performance throughout setup, conduct, and close-out.