Remote Oncology Clinical Project Manager

Syneos Health, Inc.

Washington

Hybrid

USD 120,000 - 135,000

Full time

14 days+

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Benefits offered by this job

Health benefits

401k

Employee stock purchase plan

Car allowance

Job summary

Syneos Health, Inc. is seeking a Clinical Project Manager II – Oncology for a fully remote US-based role. You will lead global oncology trials, collaborating with cross-functional teams, vendors, and international stakeholders to drive operational execution and timely delivery.

Candidates should have 3+ years of global oncology PM experience, strong leadership, regulatory knowledge and proficiency with CTMS/eTMF. This role offers competitive compensation and comprehensive benefits.

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.
Vendor management experience required.
Strong understanding of clinical trial operations and study lifecycle management.
Experience supporting Phase I–IV oncology studies.
Strong working knowledge of ICH-GCP guidelines and clinical research regulations.
Proficiency with Microsoft Office Suite.
Ability to work effectively within global, cross-functional matrix organizations.

Responsibilities

Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials.
Lead day-to-day study management activities across startup, conduct, maintenance, and 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 proactively identify areas requiring intervention.
Ensure inspection readiness and compliance with applicable regulations and sponsor requirements.
Collaborate with stakeholders across Clinical Operations, Data Management, Biostatistics, Medical Monitoring, Regulatory Affairs, Safety, Supply Chain, and Quality.
Contribute to study status reporting and executive-level communications.
Support achievement of study milestones, enrollment targets, database locks, and study closeout activities.