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Oncology Project Manager Jobs (NOW HIRING)

Medpace, Inc.

Oncology Project Manager

Cincinnati, OH · On-site

Job Summary Our imaging services are growing rapidly, and we are currently seeking a full-time, office based Oncology Project Manager to join our team. If you want an exciting career where you use ...

Medpace, Inc.

Oncology Project Manager

Denver, CO · On-site +1

$80K - $120K/yr

Job Summary Our imaging services are growing rapidly, and we are currently seeking a full-time, office based Oncology Project Manager to join our team. If you want an exciting career where you use ...

Medpace, Inc.

Oncology Project Manager

Denver, CO · On-site

$80K - $120K/yr

Job Summary Our imaging services are growing rapidly, and we are currently seeking a full-time, office based Oncology Project Manager to join our team. If you want an exciting career where you use ...

Medpace, Inc.

Oncology Project Manager

Cincinnati, OH · On-site +1

Job Summary Our imaging services are growing rapidly, and we are currently seeking a full-time, office based Oncology Project Manager to join our team. If you want an exciting career where you use ...

AbbVie

Project Manager - Oncology

Mettawa, IL

The Project Manager serves as a strategic partner to Oncology Commercial and Medical leaders, translating strategic priorities into actionable programs that strengthen organizational capabilities ...

AbbVie

Project Manager - Oncology

Mettawa, IL

The Project Manager serves as a strategic partner to Oncology Commercial and Medical leaders, translating strategic priorities into actionable programs that strengthen organizational capabilities ...

AbbVie

Project Manager - Oncology

Mettawa, IL · On-site

$109K/yr

The Project Manager serves as a strategic partner to Oncology Commercial and Medical leaders, translating strategic priorities into actionable programs that strengthen organizational capabilities ...

Icon plc

Project Manager (Hem/Onc)

Raleigh, NC · Remote

Project Manager (Hem/ONC)- United States- Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

ICON

Project Manager (Hem/Onc)

Blue Bell, PA · On-site

Project Manager (Hem/ONC)- United States- Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Icon plc

Project Manager (Hem/Onc)

Blue Bell, PA · Remote

Project Manager (Hem/ONC)- United States- Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Nemours Foundation

Project Manager

Jacksonville, FL

Leads and executes Hematology/Oncology strategic initiatives, including CORKM grant deliverables ... Manages project lifecycles from initiation through implementation, ensuring alignment with Hem/Onc ...

Jobtailor

Manager, Clinical Pharmacology

California, MO · On-site

$150 - $230/hr

Provides clinical pharmacology expertise to oncology project teams including planning, design, and oversight of clinical pharmacology studies * Participates in implementing model-based drug ...

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Oncology Project Manager information

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$38.5K

$102.7K

$162K

How much do oncology project manager jobs pay per year?

As of Aug 19, 2026, the average yearly pay for oncology project manager in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.

What is an oncology project manager?

An Oncology Project Manager is a professional responsible for overseeing and coordinating cancer-related clinical trials, research studies, or pharmaceutical projects. They manage timelines, budgets, and resources, ensuring all project milestones are met while adhering to regulatory and ethical standards. These managers work closely with medical professionals, regulatory agencies, and stakeholders to deliver successful oncology projects. Their role is crucial in advancing cancer research and bringing new therapies to patients efficiently and safely.

What are some common challenges oncology project managers face when coordinating clinical trials, and how can they be addressed?

Oncology Project Managers often encounter challenges such as managing complex regulatory requirements, coordinating multidisciplinary teams, and ensuring timely patient recruitment. These trials can involve multiple sites, each with its own processes and standards, which adds to the complexity. To address these challenges, effective communication, meticulous planning, and proactive risk management are essential. Building strong relationships with site staff and maintaining up-to-date knowledge of oncology trial regulations can also help ensure smooth project execution.

What are the key skills and qualifications needed to thrive as an oncology project manager, and why are they important?

To thrive as an Oncology Project Manager, you need a strong background in life sciences or healthcare, experience in project management, and knowledge of oncology clinical trials. Familiarity with clinical trial management systems (CTMS), regulatory guidelines (such as GCP and FDA regulations), and project management certifications like PMP are often required. Exceptional organizational, leadership, and communication skills help build effective teams and ensure smooth coordination among stakeholders. These skills and qualifications are essential for managing complex oncology projects efficiently, ensuring compliance, and delivering successful trial outcomes.

What is the difference between Oncology Project Manager vs Clinical Research Coordinator?

AspectOncology Project ManagerClinical Research Coordinator
CredentialsTypically requires a bachelor’s degree in life sciences, project management certification often preferredRequires a bachelor’s degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentManages multiple oncology clinical trials, oversees teams, and coordinates with stakeholdersConducts daily trial activities, recruits patients, and collects data at clinical sites
Employer & IndustryPharmaceutical companies, biotech firms, research institutionsHospitals, research centers, academic institutions

The Oncology Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day trial activities at clinical sites. Both roles require relevant certifications and work within the oncology research industry, but their responsibilities and scope differ significantly.

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Cities with the most Oncology Project Manager job openings:

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Oncology Project Manager jobs near you
Infographic showing various Oncology Project Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $102,682 per year, or $49.4 per hour.

Oncology Project Manager

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, Retirement, PTO

Re-posted 27 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 73 rated research

Job description

Job Summary
Our imaging services are growing rapidly, and we are currently seeking a full-time, office based Oncology Project Manager to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities
  • The primary role of the Project Manager is to provide tactical management, administration, and leadership to Medpace Core Laboratory's project teams in order to ensure that the project proceeds on time and within budget as it relates to central imaging, ECG, and/or remote biosensing technology data management;
  • Utilize study management tools to track: site start-up activities, site performance issues, submission of data, etc.;
  • Responsible for the delivery of Medpace Core Laboratory services to sponsors within expected timelines and budget;
  • Conducts ongoing study team meetings;
  • Performs scheduling of activities and deliverables in conjunction with client and internal customers;
  • Provides timely notification of all appropriate parties with deviations from timelines and/or deliverables;
  • Conducts regular communication with team members, formal and informal, regarding study status or any other changes;
  • Maintain ongoing Sponsor contact for project issues; serve as primary contact for Sponsor, internal project team and external imaging-related vendors.

Qualifications
  • Advanced degree with a focus in oncology, cell biology, biomedical engineering, physics or related field with knowledge of imaging techniques,
  • Knowledge and experience with Imaging interpretation and acquisition required,
  • Prior experience in Imaging Core Lab is preferred,
  • Knowledge and understanding of basic oncology imaging response criteria, RECIST 1.1, Lugano, and RANO; and
  • Familiarity and basic understanding of CT, MRI, PET, and SPECT/CT.

Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience
    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

What Medpace employees say

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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