Remote Oncology Clinical Project Manager

Syneos Health/ inVentiv Health Commercial LLC

New Jersey

Remote

USD 120,000 - 135,000

Full time

14 days+

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Job summary

Syneos Health is seeking an experienced Clinical Project Manager II in 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 excellence and timely delivery.

Candidates should have 3+ years in global oncology CPM, strong ICH-GCP knowledge, and hands-on leadership across multiple regions.

Qualifications

Bachelor's degree in a scientific, healthcare, or related field.
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 understanding of clinical trial operations and study lifecycle management.
Experience supporting Phase I, Phase II, Phase III, and/or Phase 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

Drive the operational execution and delivery of global oncology trials, ensuring they are conducted efficiently and in compliance.
Lead day-to-day study management 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 meetings and drive action item follow-up.
Support study-level planning, forecasting, and operational strategy execution.
Monitor study performance metrics and proactively identify areas needing 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.