Senior CRA – Remote Site Monitoring Leader

Parexel; Montpelier (VT); On-site; USD 95,000 - 130,000; Full time

Job summary

Parexel is seeking a Senior Clinical Research Associate to manage site monitoring, initiation, and close-out activities for assigned sites in the US. The role emphasizes patient safety, GCP compliance, and collaboration with the SCP and study team to ensure timely, high-quality trial delivery.

The Sr CRA will travel frequently (60-80%), monitor sites (onsite and remote as needed), review data, resolve issues, and support training of site staff to maintain protocol adherence and study integrity

Qualifications

• Bachelor’s degree in life sciences or related field.
• Experience in clinical research and monitoring.
• Ability to work in a matrix team environment.
• Strong understanding of GCP and regulatory requirements.

Responsibilities

• Ensure proper conduct of clinical trials per SMP and GCP.
• Manage site activation through database lock with timelines and quality deliverables.
• Serve as primary contact for investigator sites; coordinate with SCP.
• Interface with study team and vendors to ensure smooth information flow.
• Provide site training and address protocol questions from site staff.

Skills

Clinical trial knowledge

Monitoring experience

English fluent

Travel ready

Driver's license

Education

Bachelor's degree in life sciences

Job description

Parexel is seeking a Senior Clinical Research Associate to manage site monitoring, initiation, and close-out activities for assigned sites in the US. The role emphasizes patient safety, GCP compliance, and collaboration with the SCP and study team to ensure timely, high-quality trial delivery.

The Sr CRA will travel frequently (60-80%), monitor sites (onsite and remote as needed), review data, resolve issues, and support training of site staff to maintain protocol adherence and study integrity