Senior CRA - Remote Site Monitoring Lead

Parexel; Lansing (MI); On-site; USD 90,000 - 120,000; Full time

Job summary

Parexel FSP in the United States is seeking a Senior Clinical Research Associate (Sr. CRA) to manage investigator sites, monitor trials, and ensure quality and patient safety in alignment with GCP and client standards.

The Sr. CRA will liaise with the Site Care Partner and study team to ensure site activation, monitoring, recruitment support, data integrity, and eventual close-out of trials across multiple sites.

Qualifications

• Bachelor’s degree in life sciences or equivalent required.
• Five or more years of clinical monitoring experience preferred for Sr. CRA roles.
• Fluent in English and local language(s) where you will work.

Responsibilities

• Oversee site monitoring from activation through database lock to ensure patient safety and data quality.
• Manage investigator sites and relationships to support enrollment, data release, and study timelines.
• Coordinate with Study Team, SCP, and QA to address protocol questions and site issues.
• Monitor safety events and ensure timely reporting and documentation in the TMF.
• Provide training and coaching to site staff to maintain GCP compliance and study integrity.

Skills

Clinical trial monitoring

ICH/GCP

FDA regulations

Site management

Communication

Education

Bachelor's degree in life sciences

Professional degree in life sciences (nursing, pharmacy, medical)

Job description

Parexel FSP in the United States is seeking a Senior Clinical Research Associate (Sr. CRA) to manage investigator sites, monitor trials, and ensure quality and patient safety in alignment with GCP and client standards.

The Sr. CRA will liaise with the Site Care Partner and study team to ensure site activation, monitoring, recruitment support, data integrity, and eventual close-out of trials across multiple sites.