Senior CRA - Oncology Trials (Remote)

Parexel; Helena (MT); Remote; USD 90,000 - 120,000; Full time

Job summary

Parexel is seeking a capable Clinical Site Monitor to oversee monitoring activities from site activation through database lock, ensuring adherence to SMP, GCP, and client standards. This role emphasizes Oncology experience and global trial exposure.

The successful candidate will train site personnel, enable site development, and manage site communications with the SCP and study team, including recruitment support and risk mitigation.

Qualifications

• Strong knowledge of clinical trial methodologies and regulatory requirements (ICH-GCP).
• Minimum 3 years monitoring experience in clinical research sites (2 years in Oncology preferred).
• Experience with site management, patient safety and risk remediation.

Responsibilities

• Oversee monitoring from site activation to database lock in compliance with SMP and applicable laws.
• Serve as primary contact for investigator sites and coordinate with SCP for site quality.
• Coordinate with the study team, vendors and sites for information flow and issue resolution.
• Lead site development and training to ensure protocol compliance and patient safeguarding.
• Support enrollment efforts and address recruitment issues with investigators.

Skills

ICH/GCP knowledge

Monitoring experience

Oncology experience

Global clinical trials

English fluency

Travel readiness

Driver’s license & passport

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking a capable Clinical Site Monitor to oversee monitoring activities from site activation through database lock, ensuring adherence to SMP, GCP, and client standards. This role emphasizes Oncology experience and global trial exposure.

The successful candidate will train site personnel, enable site development, and manage site communications with the SCP and study team, including recruitment support and risk mitigation.