Clinical Project Manager - Oncology (Client Dedicated/Remote)

1001 Syneos Health, LLC; North Carolina; Hybrid; USD 120,000 - 135,000; Full time

Benefits offered by this job

Health benefits

401k

Employee Stock Purchase Plan

Flexible PTO and sick time

Company car or car allowance

Job summary

Syneos Health is hiring a Clinical Project Manager to lead global oncology trials, coordinating across cross-functional teams from startup to closeout. The role emphasizes vendor oversight, timelines, risk management, and regulatory readiness, with extensive collaboration across Clinical Operations and biostatistics.

The ideal candidate has 3+ years in global oncology project management, a strong understanding of ICH-GCP, and experience working in a multi-country environment.

Qualifications

• Bachelor’s degree in a scientific, healthcare, or related field is required.
• 3+ years of Clinical Project Management experience supporting global oncology trials.
• Experience across multiple countries and regions (NA, Europe, APAC, LATAM).
• Vendor management experience required.
• Strong knowledge of ICH-GCP guidelines and regulatory requirements.
• Proficiency with Microsoft Office Suite.
• Ability to function within global, cross-functional matrix organizations.

Responsibilities

• Support and partner with Clinical Study Leads and cross-functional study teams on global oncology trials.
• Lead day-to-day study management across startup, conduct, maintenance and closeout.
• Manage study timelines, deliverables, risks, and issue resolution.
• Oversee external vendors, CROs, labs, imaging and specialty providers.
• Coordinate CTT meetings and follow-up on actions.
• Support study planning, forecasting, and operational strategy execution.
• Monitor study performance metrics and interventions as needed.
• Ensure inspection readiness and regulatory sponsor compliance.
• Collaborate across Clinical Operations, Data Management, Biostatistics, Medical Monitoring, Regulatory Affairs, Safety, Supply Chain and Quality.
• Contribute to study status reporting and executive communications.
• Support milestones, enrollment targets, database locks, and closeout activities.
• Travel up to 25%.

Education

Bachelor's degree in science/healthcare

Tools

CTMS

eTMF

IRT/RTSM

Clinical data review platforms

Job description

About Syneos Health

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 centre 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

What you’ll do

• 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
• Travel up to 25%

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

Benefits

• 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.

Salary Range $120,000-135,000

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.

Learn more about Syneos Health.

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. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.