Remote Oncology Clinical Program Manager

Syneos Health, Inc.; Idaho; Hybrid; USD 120,000 - 135,000; Full time

Job summary

Syneos Health, Inc. is seeking a Clinical Project Manager II – Oncology for a fully remote US-based role. You will lead operational delivery of global oncology trials, coordinating cross-functional teams, vendors and international sites to ensure timelines and quality.

Candidates should have 3+ years of CPM experience in global oncology, experience across multiple countries, and strong ICH-GCP knowledge. Proficiency with CTMS, eTMF, and RTMS is preferred.

Qualifications

• Bachelor's degree in a scientific, healthcare, or related field is required.
• 3+ years of Clinical Project Management experience supporting global oncology clinical trials.
• Experience managing studies across multiple countries and regions (North America, Europe, Asia-Pacific, Latin America, or other global regions).
• Vendor management experience required.
• Strong working knowledge of ICH-GCP guidelines and clinical research regulations.

Responsibilities

• Lead global oncology trials across multiple indications and phases.
• Oversee day-to-day study management from startup to closeout.
• Manage study timelines, deliverables, risks, and issue resolution.
• Oversee external vendors, CROs, central laboratories, imaging vendors, and specialty providers.
• Coordinate Clinical Trial Team (CTT) meetings and drive action item follow-up.
• Support study-level planning, forecasting, and operational strategy execution.
• Monitor study performance metrics and interventions as needed.
• Ensure inspection readiness and regulatory compliance.

Skills

Clinical Project Management

Global oncology

Vendor management

Regulatory compliance

Cross-functional teamwork

MS Office

Education

Bachelor's degree in science/healthcare

Tools

CTMS

eTMF

IRT/RTSM

Job description

Syneos Health, Inc. is seeking a Clinical Project Manager II – Oncology for a fully remote US-based role. You will lead operational delivery of global oncology trials, coordinating cross-functional teams, vendors and international sites to ensure timelines and quality.

Candidates should have 3+ years of CPM experience in global oncology, experience across multiple countries, and strong ICH-GCP knowledge. Proficiency with CTMS, eTMF, and RTMS is preferred.