Senior CRA: Remote Site Monitoring Lead

Parexel; Pierre (SD); On-site; USD 90,000 - 140,000; Full time

Job summary

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to join our US-based team. The Sr.

CRA will oversee site management, monitoring, and close-out of investigative sites to ensure patient safety and data quality in accordance with GCP, ICH, and client standards. Responsibilities include monitoring plan adherence, site activation through database lock, coordinating with the Site Care Partner and study team, and ensuring timely reporting and issue resolution.

Qualifications

• Minimum 3 years of clinical research site monitoring experience.
• Must be fluent in English and the local language of the country they will work in.
• Travel 60–80% within area and possibly international.

Responsibilities

• Oversee monitoring responsibilities and study conduct.
• Manage site activation through database lock with quality deliverables.
• Serve as primary contact for investigator sites and coordinate with SCP.

Skills

ICH/GCP knowledge

FDA/regulatory knowledge

Clinical monitoring experience

Global trial experience

Education

Bachelor's degree in life sciences

Job description

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to join our US-based team. The Sr.

CRA will oversee site management, monitoring, and close-out of investigative sites to ensure patient safety and data quality in accordance with GCP, ICH, and client standards. Responsibilities include monitoring plan adherence, site activation through database lock, coordinating with the Site Care Partner and study team, and ensuring timely reporting and issue resolution.