Description
Clinical Project Manager - Oncology (Client Dedicated/Remote)

Job Responsibilities

CLINICAL PROJECT MANAGER II - ONCOLOGY
Sponsor Dedicated | Remote - United States

Are you passionate about advancing cancer research and bringing innovative therapies to patients worldwide? 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.

WHAT YOU'LL DO

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.

Key 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 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

WHAT YOU WILL BRING

Required 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 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

ONCOLOGY THERAPEUTIC AREA EXPERIENCE

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

• Lung cancer (NSCLC, SCLC)
• Melanoma
• Renal cell carcinoma (kidney)
• Bladder cancer
• Head & neck squamous cell carcinoma
• Triple-negative breast cancer
• Cervical cancer
• Gastric and gastroesophageal cancers
• Esophageal cancer
• Hepatocellular carcinoma (liver)
• Endometrial cancer
• Ovarian cancer
• Colorectal cancer
• Biliary tract cancer
• Prostate cancer
• Urothelial carcinoma
• Hematologic malignancies (multiple myeloma, lymphoma, leukemia)
• Antibody-drug conjugates (ADCs)
• Personalized cancer vaccines
• KRAS inhibitors
• T-cell engagers
• Cell-directed immunotherapies

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

PREFERRED QUALIFICATIONS

• Experience independently leading global oncology studies
• Experience supporting complex, multi-regional Phase II and Phase III programs
• Experience with early-phase oncology studies (Phase I/Ib)
• 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

KEY SKILLS & COMPETENCIES

• Strong project management and organizational skills
• Excellent communication and stakeholder management abilities
• Proven ability to manage multiple priorities in a fast-paced environment
• Strong risk identification and mitigation capabilities
• 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

CLINICAL PHASE EXPERIENCE

We welcome candidates with experience supporting:

• Phase I / First-in-Human Studies
• Phase I/Ib Dose Escalation Studies
• Phase II Proof-of-Concept Studies
• Phase II/III Registrational Studies
• Phase III Global Pivotal Trials
• Phase IV and Post-Marketing Studies

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

WHY JOIN US?

• 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
• Enjoy the flexibility of a fully remote US-based role
• 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.

Salary Range $120,000-135,000

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.

At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range:

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.

Summary
Roles within Clinical Project Management job family are responsible for planning, directing, creating and communicating clinical study time-lines. Gathers input from cross-functional teams and creates plans that help the team produce deliverables on schedule. Ensures consistency of clinical study and processes across clinical trials, overseeing and resolving operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets. Ensures studies are conducted within clinical trial protocols, monitoring progress and following up with team members and line managers when issues develop. Implements and prepares the clinical development strategy as outlined by the clinical teams. May develop trial recruitment strategies. Impact and Contribution Includes executives as well as managers, supervisors and team leads providing strategic vision and/or tactical direction across a discipline and/or broader organization. The majority of time is spent overseeing their area of responsibility, planning, prioritizing, and/or directing the responsibilities of employees. Goal are achieved through management of process, policy, and performance of direct and/or indirect reports. Supervises experienced support employees and/or entry individual contributors. Delivers operational results that have moderate impact on the immediate achievement of results for the team. Broad job knowledge in an operational, administrative and/or specialized field, adapts new procedures, techniques, tools, etc. Understands basic management approaches such as work scheduling, prioritizing, coaching and process execution.