Senior Clinical Research Associate (Remote, Western US)

Parexel; Montpelier (VT); Sur place; USD 70 000 - 100 000; Plein temps

Résumé du poste

Parexel is seeking a Clinical Research Associate (CRA) to manage investigator sites, monitor trials, and support close-out, ensuring patient safety and data quality in line with GCP and sponsor standards.

You will collaborate with the Site Care Partner and study team, handle site activation to database lock, travel 60–80%, and hold a life sciences degree with English fluency. This US-based role offers exposure to diverse studies and requires strong communication and problem-solving skills.

Qualifications

• Extensive knowledge of clinical trial methodologies and regulatory standards.
• Experience monitoring clinical trial sites and managing site relationships.
• Ability to travel 60-80% and work across multiple sites.

Responsabilités

• Ensure proper conduct of clinical trials in accordance with SMP, SOPs and GCP.
• Manage site activation through to database lock with quality deliverables.
• Serve as primary contact for investigator sites and coordinate with SCP.
• Conduct onsite or remote monitoring and address SAE/AE reporting.
• Prepare required reports and close-out activities within timelines.

Connaissances

Clinical trial knowledge

ICH/GCP

FDA regulations

Site monitoring

Travel readiness

Driver’s license & passport

English fluency

Formation

Bachelor’s degree in life sciences or related field

Description du poste

Parexel is seeking a Clinical Research Associate (CRA) to manage investigator sites, monitor trials, and support close-out, ensuring patient safety and data quality in line with GCP and sponsor standards.

You will collaborate with the Site Care Partner and study team, handle site activation to database lock, travel 60–80%, and hold a life sciences degree with English fluency. This US-based role offers exposure to diverse studies and requires strong communication and problem-solving skills.