CLINICAL PROJECT MANAGER II - ONCOLOGY

First Job Previous Job 2,374 of 10,000 More Like This Salary Not Available Position range in Kansas City, MO-KS Metropolitan Statistical Area $78k•$130k Per Year

CLINICAL PROJECT MANAGER II

•ONCOLOGY Syneos Health/ inVentiv Health Commercial LLC

Occupation:

Project Management Specialists

Location:

Kansas City, MO•64118

Job Type:

Full Time (30 Hours or More)

Posted:

06/23/2026 Positions available: 1

Source:

FileImport•Syneos Health/ inVentiv Health Commercial LLC

Web Site:

commercialcareers.syneoshealth.com

Expires:

08/25/2026 Job #: 25108969MO Job Requirements and Properties Help for Job Requirements and Properties. Opens a new window. Work Onsite Full Time Schedule Full Time Job Description Help for Job Description. Opens a new window.

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

BRINGRequired Qualifications Bachelor's ...For full information see follow application link.