Syneos Health

Clinical Project Manager - Oncology (Client Dedicated/Remote)

$120K–$135KFull-time · Remote, UT
✓ Verified live on the employer's own system · added 36 days ago
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Mid-level · 3+ yrs exp

Requirements

Education: Bachelor's degree or related field

Experience: 3+ years

Skills & tools

OperationsTeam LeadershipProject ManagementManagementMaintenanceFinancial AnalysisRegulatory ComplianceLogistics
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Full job description

We are seeking experienced Clinical Project Managers with strong global oncology clinical trial experience to join a high-performing sponsor-dedicated team supporting a diverse portfolio of oncology studies across multiple indications and phases of development.

This is a fully remote, US-based opportunity where you will play a critical role in the operational leadership and execution of global clinical trials. We are specifically seeking professionals with 3+ years of hands-on Clinical Project Management experience leading global oncology studies and collaborating with cross-functional teams, vendors, and international stakeholders.

As a Clinical Project Manager II, you will help drive the operational execution and delivery of global oncology clinical trials, ensuring studies are conducted efficiently, compliantly, and according to established timelines.

- Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials

- Lead day-to-day study management activities across study 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

- 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)

- 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

- Ability to work effectively within global, cross-functional matrix organizations

Candidates should have direct clinical trial experience supporting one or more oncology indications:

- Hematologic malignancies (multiple myeloma, lymphoma, leukemia)

Candidates should be prepared to discuss the indications supported, study phases, geographic scope, and their specific responsibilities on each program.

- Experience supporting complex, multi-regional Phase II and Phase III programs

- Experience with immuno-oncology, targeted therapies, cell therapy, or hematologic malignancies

- Familiarity with CTMS, eTMF, IRT/RTSM, and clinical data review platforms

- Experience working in sponsor-dedicated or FSP environments

- Excellent communication and stakeholder management abilities

- Proven ability to manage multiple priorities in a fast-paced environment

- Detail-oriented with a focus on quality, compliance, and execution

- Strong collaboration skills across global teams and functions

- Ability to influence without direct authority and drive accountability across study teams

Experience supporting global, multi-country oncology programs through multiple phases of development is highly preferred.

- Work on innovative oncology programs advancing new treatment options for cancer patients worldwide

- Support cutting-edge therapies across solid tumors, hematologic malignancies, immuno-oncology, and cell and gene therapy

- Join a collaborative, sponsor-dedicated team focused on operational excellence

- Expand your impact across global clinical development programs and contribute to bringing life-changing therapies to patients

If you are an experienced Oncology Clinical Project Manager with 3+ years of global clinical trial management experience and a passion for advancing cancer research, we would love to hear from you.

We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.

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This posting was published by Syneos Health on their own careers system and is shown here with a direct link to apply there. Employers: for corrections or removal, contact jobs@veritahire.com.