Clinical Trial Project Manager - Oncology/Hematology (Sign-On Bonus Eligible)
Job Locations
United States-OH-Cincinnati | United States | United States-TX-Irving
(Dallas) | United States-CO-Denver
Category
Clinical Trial Management
Job Summary
Medpace is the leading CRO for Biotech companies and is continuing to add
established Clinical Trial Managers and Project Managers with a focus on
Oncology/Hematology to join our Clinical Trial Management Group. We have
just expanded our campus in Cincinnati and have offices in Dallas and
Denver, and provide remote flexibility with relevant experience. We offer a
very competitive salary/bonus program, plus equity grants which have
become very lucrative for our associates.
Responsibilities
Manage and provide accountability for day-to-day operations of the project,
as defined by the contract and according to ICH/GCP and all other applicable
laws, rules, and regulations;
Serve as primary Sponsor contact for operational project-specific issues and
study deliverables;
Maintain in depth knowledge of protocol, therapeutic area, and indication;
Provide cross-functional oversight of internal project team members and
deliverables, which includes ensuring all necessary project-specific
training is provided;
Review and provide input for study protocol, edit check specifications,
data analysis plan, and final study report, when applicable;
Develop operational project plans;
Manage risk assessment and execution;
Responsible for management of study vendor; and
Manage site quality, including direct supervision of project Clinical
Research Associates and monitoring deliverables.
Qualifications
Bachelor's degree in a health-related field; Advanced degree in a
health-related field preferred;
Experience in Phases 1-4; Phases 2-3 preferred;
5+ years as a project/clinical trial manager within a CRO- required for
home-based;
Management of overall project timeline; and
Strong leadership skills.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO).
We provide Phase I-IV 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 its
scientific and disciplined approach. We leverage local regulatory and
therapeutic expertise across all major areas including oncology,
cardiology, metabolic disease, endocrinology, central nervous system,
anti-viral and anti-infective. Headquartered in Cincinnati, Ohio,
employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the
lives of countless patients and families who face hundreds of diseases across
all key therapeutic areas. The work we do today will improve the lives of
people living with illness and disease in the future.
Cincinnati Perks
Cincinnati Campus Overview
Hybrid work-from-home options (dependent upon position and level)
Competitive PTO packages, starting at 20+ days
Competitive compensation and benefits package
Flexible work schedule
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Community involvement with local nonprofit organizations
Discounts on local sports games, fitness gyms and attractions
Modern, ecofriendly campus with an on-site fitness center
Structured career paths with opportunities for professional growth
Discounted tuition for UC online programs
Awards
Recognized by Forbes as one of America's Most Successful Midsize Companies
in 2021, 2022, 2023 and 2024
Continually recognized with CRO Leadership Awards from Life Science Leader
magazine based on expertise, quality, capabilities, reliability, and
compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if inte ested,
you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets