CLINICAL PROJECT MANAGER II – ONCOLOGY

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a functional service provider partnership or a full‑service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate about changing lives.

Job 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.

Required 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.

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.

Oncology Therapeutic Area Experience
Solid Tumors

Non‑Small Cell Lung Cancer (NSCLC)

Small Cell Lung Cancer (SCLC)

Breast Cancer

Ovarian Cancer

Cervical Cancer

Endometrial Cancer

Prostate Cancer

Colorectal Cancer

Pancreatic Cancer

Gastric Cancer

Esophageal Cancer

Hepatocellular Carcinoma (HCC)

Melanoma

Renal Cell Carcinoma (RCC)

Bladder Cancer

Head and Neck Cancer

Thyroid Cancer

Sarcoma

Gynecologic Malignancies

Hematologic Malignancies

Multiple Myeloma

Acute Myeloid Leukemia (AML)

Acute Lymphoblastic Leukemia (ALL)

Chronic Lymphocytic Leukemia (CLL)

Chronic Myeloid Leukemia (CML)

Hodgkin Lymphoma

Non‑Hodgkin Lymphoma

Myelodysplastic Syndromes (MDS)

Myeloproliferative Neoplasms (MPN)

Advanced Therapeutic Areas

Immuno‑Oncology

Cell and Gene Therapy

CAR‑T Programs

Bispecific Antibodies

Antibody Drug Conjugates (ADCs)

Precision Medicine / Biomarker‑Driven Studies

Clinical Phase Experience

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

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.

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 U.S.‑based role.

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

Salary Range
USD 120,000 – 135,000. Actual salary will vary based on candidate qualifications and other factors.

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.

Get to Know Syneos Health
Over the past 5 years, we have worked with 94% of all novel FDA‑approved drugs, 95% of EMA‑authorized products, and over 200 studies across 73,000 sites and 675,000+ trial patients.

Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company may assign other tasks and duties at its discretion and may consider equivalent experience and education. The Company is committed to compliance with the Americans with Disabilities Act and will provide reasonable accommodations as needed.

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