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 that 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 to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.
Job Responsibilities
CLINICAL PROJECT MANAGER II - ONCOLOGYSponsor 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
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, including but not limited to:
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
Candidates should be prepared to discuss the indications supported, study phases, geographic scope, and their specific responsibilities on each... For full info follow application link.
