Clinical Trial Project Manager - Cincinnati, OH

Medpace; Cincinnati (OH); On-site; USD 80,000 - 110,000; Full time

Job summary

An established industry player in clinical research is seeking a Clinical Trial Project Manager to lead projects in Cincinnati. This role offers an exciting opportunity to manage diverse clinical trials across various therapeutic areas, ensuring compliance with regulatory standards. The company prides itself on its supportive culture and commitment to employee growth, providing competitive compensation and a flexible work environment. Join a team dedicated to making a meaningful impact on patient lives through innovative research and development. If you are passionate about clinical trials and looking for a rewarding career, this position is perfect for you.

Benefits

Flexible work environment

Competitive PTO packages, starting at 20+ days

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Discounts on local sports games and attractions

Modern, ecofriendly campus with an on-site fitness center

Discounted tuition for UC online programs

Qualifications

• 5+ years as a project/clinical trial manager within a CRO.
• Experience in Phases 1-4; Phases 2-3 preferred.

Responsibilities

• Manage day-to-day operations of clinical trial projects.
• Serve as primary Sponsor contact for project-specific issues.
• Develop operational project plans and manage risk assessments.

Skills

Project Management

Leadership

Clinical Trial Management

Risk Assessment

Education

Bachelor's degree in a health-related field

Advanced degree in a health-related field

Job description

Clinical Trial Project Manager - Cincinnati, OH

Job Locations

United States-OH-Cincinnati | United States-OH-Cincinnati

Category

Clinical Trial Management

Job Summary

Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Cincinnati, OH. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. 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
• 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
• 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
• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• 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

• Named a Top Workplace in 2024 by The Cincinnati Enquirer

• 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 interested, you will be contacted with details for next steps.

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