Senior Clinical Program Manager, Cancer Research Portfolio

GAP SOLUTIONS INC; Bethesda (MD); On-site; USD 125,000 - 185,000; Full time

Job summary

GAP Solutions Inc. is seeking an Experienced Clinical Program Manager to support the National Cancer Institute within NIH.

The role requires managing clinical research portfolios, coordinating with investigators, regulatory offices, and partnering institutions to ensure efficient study execution and governance. Responsibilities include developing work plans, tracking milestones, overseeing budgets, and maintaining robust risk mitigation strategies across multi-site trials.

Qualifications

• Master’s degree in Health and Medical Administration or related field.
• SOCRA, FAC-P/M, FAC-COR, PMP, and ACRP certifications.
• Experience with clinical trial management systems.
• Experience supporting NIH/NCI or federally funded programs.

Responsibilities

• Provide comprehensive management and oversight of assigned clinical research portfolios.
• Develop and maintain project management plans for clinical research projects.
• Monitor project schedules, timelines, deliverables, dependencies, and milestones.
• Track portfolio performance metrics and report progress to leadership.
• Collaborate with investigators and regulatory staff to ensure compliance and timely study milestones.

Skills

Clinical trial management

Regulatory compliance

Stakeholder communication

Portfolio coordination

Education

Master’s degree in Health/Medical Administration or related field

SOCRA Certification

FAC-P/M Certification

FAC-COR Certification

PMP Certification

ACRP Certification

Tools

CTMS (electronic trial management systems)

Job description

GAP Solutions Inc. is seeking an Experienced Clinical Program Manager to support the National Cancer Institute within NIH.

The role requires managing clinical research portfolios, coordinating with investigators, regulatory offices, and partnering institutions to ensure efficient study execution and governance. Responsibilities include developing work plans, tracking milestones, overseeing budgets, and maintaining robust risk mitigation strategies across multi-site trials.