Senior CRA: Remote Site Monitoring Leader

Parexel; Annapolis (MD); Hybrid; USD 90,000 - 130,000; Full time

Job summary

Parexel FSP is seeking a Senior Clinical Research Associate (Sr. CRA) in the US to oversee site monitoring, activation, and close-out of trials, ensuring patient safety and data quality in line with GCP and SOPs.

The Sr. CRA will manage investigator site relationships, coordinate with the Site Care Partner and study team, and travel extensively (60–80%) to sites to support enrollment and monitoring activities.

Qualifications

• Extensive knowledge of clinical trial methodologies and regulatory expectations.
• Experience monitoring in clinical research with a focus on quality and patient safety.
• Ability to work across sites and with cross-functional teams.

Responsibilities

• Ensure proper conduct of trials per SMP, GCP, and client standards.
• Manage site activation through database lock with timely, quality deliverables.
• Serve as primary contact for investigator sites; escalate to SCP as needed.
• Coordinate with the study team to ensure smooth information flow.
• Monitor safety signals and ensure timely reporting of AEs/SAEs.

Skills

Clinical Monitoring

GCP compliance

FDA regulations

Oncology experience

High travel capacity

Education

Bachelor's degree in life sciences

Job description

Parexel FSP is seeking a Senior Clinical Research Associate (Sr. CRA) in the US to oversee site monitoring, activation, and close-out of trials, ensuring patient safety and data quality in line with GCP and SOPs.

The Sr. CRA will manage investigator site relationships, coordinate with the Site Care Partner and study team, and travel extensively (60–80%) to sites to support enrollment and monitoring activities.