Clinical Trial Project Manager - Cardiovascular, Renal, Gastrointestinal

Medpace; Cincinnati (OH); Hybrid; USD 80,000 - 120,000; Full time

Job summary

Join a leading CRO for Biotech companies as a Clinical Trial Project Manager in Cincinnati, focusing on Cardiovascular, Renal, and Gastrointestinal areas. This role offers a competitive salary and bonus program, along with equity grants. You'll manage project operations, oversee internal teams, and ensure compliance with regulations. Enjoy a flexible work environment, generous PTO, and opportunities for professional growth. Be part of a mission-driven team making a significant impact on the lives of patients. If you're passionate about clinical trials and looking for a rewarding career, this is the opportunity for you.

Benefits

Flexible work environment

Competitive PTO packages

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Discounts on local sports games

Modern, ecofriendly campus

Discounted tuition for UC online programs

Qualifications

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

Responsibilities

• Manage day-to-day operations of the project according to ICH/GCP.
• Serve as primary contact for operational project-specific issues.

Skills

Project Management

Leadership Skills

Clinical Trial Management

Regulatory Knowledge (ICH/GCP)

Education

Bachelor's Degree in Health-related Field

Advanced Degree in Health-related Field

Job description

Clinical Trial Project Manager - Cardiovascular, Renal, Gastrointestinal

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 Cardiovascular, Renal, and Gastrointestinal therapeutic areas 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
• 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.

EO/AA Employer M/F/Disability/Vets