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Oncology (Client Dedicated/Remote) Company\tSyneos Health/ inVentiv Health Commercial LLC\nLocation\tBillings, MT\nDate Posted\t09/24/2026\nDescription Experience Required 3
20 years\nMinimum Education Required Bachelor's Degree\nCompensation $ / yearly\nHours Per Week 40\nNumber Of Positions 1\nJob Description Clinical Project Manager
Oncology (Client Dedicated/Remote) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.

We translate unique clinical, medical affairs andmercial insights into oues 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 MATTERS EVERYW

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 aremitted to our Total Self culture

w 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 thepany 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 w 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, with up to 25% travel, w 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,pliantly, 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 andpliance 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-levelmunications Support achievement of study milestones, enrollment targets, database locks, and study closeout activities Travel up to 25%

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 supportingplex, 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 Excellentmunication 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,pliance, 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 wee 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] uing opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role be 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 apany 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 earnmissions/bonus based onpany 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 w you work. Syneosplies 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,petencies, and proficiency for the role. 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. No matter what your role is, you'll take the initiative and challenge the status quo with us in a highlypetitive and ever-changing environment. Learn more about Syneos Health. syneoshealth 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 in should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained in is intended to fullyply 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. The Company ismitted topliance with the Americans with Disabilities Act, including the provision of reasonable amodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Is this a registered apprenticeship? False\nPlace of Work On-site Requisition

ID 25108969

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Clinical Project Manager

Oncology (Client Dedicated/Remote) Company\tSyneos Health/ inVentiv Health Commercial LLC
Location\tBillings, MT
Date Posted\t09/24/2026
Description Experience Required 3
20 years
Minimum Education Required Bachelor's Degree
Compensation $ / yearly
Hours Per Week 40
Number Of Positions 1
Job Description Clinical Project Manager
Oncology (Client Dedicated/Remote) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.

WORK MATTERS EVERYW

w 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 thepany 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 w 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?

WHAT YOU'LL DO

WHAT YOU WILL BRING

ONCOLOGY THERAPEUTIC AREA EXPERIENCE

PREFERRED QUALIFICATIONS

KEY SKILLS & COMPETENCIES

CLINICAL PHASE EXPERIENCE

WHY JOIN US?

Place of Work On-site Requisition

ID 25108969

Job Type Full Time

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Find & Apply For Clinical Research Manager Jobs in Billings, Montana

Clinical Project Manager - Oncology (Client Dedicated/Remote)