Senior Clinical Research Associate (Oncology) – Remote

Parexel; Richmond (VA); Remote; USD 85,000 - 140,000; Full time

Job summary

Parexel is seeking an experienced Clinical Site Monitor to oversee monitoring activities across oncology and non-oncology studies in the United States. You will ensure trials comply with SMP, GCP, and client standards while maintaining timelines and data integrity.

This role covers site activation through database lock, patient safety oversight, and collaboration with SCP, the study team, and investigators. Travel will be substantial (60–80%), and oncology experience is preferred.

Qualifications

• Minimum 3 years of site monitoring experience in clinical research.
• Oncology experience preferred.
• Understanding of regulatory requirements and patient safety.
• Ability to work in a matrix team and communicate effectively.

Responsibilities

• Oversee monitoring activities and study conduct per SMP and regulations.
• Coordinate site management from activation to database lock.
• Serve as main contact for investigator sites and teams.
• Ensure timely trial documentation and AE/SAE reporting.
• Support training and audit readiness with site staff.

Skills

Clinical trial monitoring

GCP/ICH compliance

Oncology experience

Global trials

Fluent English

Travel flexibility

Education

Bachelor’s degree in life sciences

Professional degree in life sciences

Job description

Parexel is seeking an experienced Clinical Site Monitor to oversee monitoring activities across oncology and non-oncology studies in the United States. You will ensure trials comply with SMP, GCP, and client standards while maintaining timelines and data integrity.

This role covers site activation through database lock, patient safety oversight, and collaboration with SCP, the study team, and investigators. Travel will be substantial (60–80%), and oncology experience is preferred.