Remote Clinical Research Associate – Oncology Trials

Parexel; Denver (CO); On-site; USD 70,000 - 120,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to act as the primary site contact and site manager across all trial phases. The role focuses on site relationships, monitoring activities, and regulatory documentation to ensure compliant study execution.

Must have direct site monitoring experience (minimum 2 years) in bio/pharma/CRO and a Bachelor’s degree in science/biology. Willingness to travel 65–75% of the time is required.

Qualifications

• Minimum 2 years of direct site monitoring experience in bio/pharma/CRO.
• Bachelor’s degree preferred with a strong emphasis in science and/or biology.

Responsibilities

• Acts as the primary site contact and site manager throughout all phases of a clinical research study.
• Develops strong site relationships and ensures continuity through all phases of the trial.
• Performs remote and on-site monitoring with adherence to ICH-GCP, sponsor SOPs, and local regulations.
• Manages regulatory documentation for study start-up, maintenance and close-out.
• Communicates issues related to protocol conduct, recruitment, retention, and quality with investigators and site staff.
• Identifies and resolves site performance, quality or compliance problems and escalates as needed.
• Maintains documentation in CTMS, eTMF and other systems per timelines.
• Contributes to CRA team knowledge as a mentor and shares best practices.
• Supports audits/inspections and participates in co-monitoring visits where appropriate.

Skills

English proficiency

Site monitoring

Communication skills

Travel willingness

Education

Bachelor’s degree in science/biology

Job description

Parexel is seeking a Clinical Research Associate to act as the primary site contact and site manager across all trial phases. The role focuses on site relationships, monitoring activities, and regulatory documentation to ensure compliant study execution.

Must have direct site monitoring experience (minimum 2 years) in bio/pharma/CRO and a Bachelor’s degree in science/biology. Willingness to travel 65–75% of the time is required.