Oncology Clinical Trials Coordinator: Lead & Compliance

Guidehouse Inc.; Bethesda (MD); On-site; USD 75,000 - 110,000; Full time

Job summary

Guidehouse Inc. in Bethesda, MD is seeking a full-time on-site Clinical Trials Operations professional with oncology trials experience. You will guide junior staff, assist with onboarding, and ensure data quality across EMR/CTMS platforms while maintaining regulatory compliance.

The role supports protocol execution, documentation, and study closeout, coordinating with IRBs and sponsors to ensure inspection readiness and data integrity in a fast-paced environment.

Qualifications

• Bachelor's degree in nursing or related field.
• Minimum 2 years oncology clinical trials experience.
• Experience with EMR and CTMS systems.

Responsibilities

• Provide guidance and training to junior staff and students.
• Onboard protocol operations and study procedures.
• Enter and validate research data in approved systems.
• Coordinate specimen handling and regulatory documentation.
• Monitor participant eligibility and protocol windows.
• Support adverse event reporting and study closeout.

Skills

EMR experience

CTMS experience

Clinical research operations

Education

Bachelor's degree in Nursing/Biological Sciences/Public Health

Job description

Guidehouse Inc. in Bethesda, MD is seeking a full-time on-site Clinical Trials Operations professional with oncology trials experience. You will guide junior staff, assist with onboarding, and ensure data quality across EMR/CTMS platforms while maintaining regulatory compliance.

The role supports protocol execution, documentation, and study closeout, coordinating with IRBs and sponsors to ensure inspection readiness and data integrity in a fast-paced environment.