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Clinical Trial Project Manager - Infectious Diseases

Medpace

Cincinnati (OH)

On-site

USD 80,000 - 110,000

Full time

6 days ago
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Job summary

An established industry player is seeking a Clinical Trial Project Manager specializing in Infectious Diseases. This role offers the opportunity to manage diverse clinical trials while ensuring compliance with regulations and maintaining high-quality standards. The position provides a flexible work environment and competitive compensation, making it an attractive opportunity for experienced professionals. Join a dedicated team committed to advancing medical research and improving patient outcomes globally. Be part of a mission-driven organization that values its employees and fosters professional growth.

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 with fitness center
Structured career paths
Discounted tuition for UC online programs

Qualifications

  • 5+ years of experience as a project/clinical trial manager within a CRO.
  • Strong leadership and management of project timelines.

Responsibilities

  • Manage day-to-day operations of clinical trials according to regulations.
  • Serve as primary contact for project-specific issues and deliverables.

Skills

Project Management
Clinical Trial Management
Leadership Skills
Regulatory Knowledge

Education

Bachelor's Degree in Health-related Field
Advanced Degree in Health-related Field

Job description







Clinical Trial Project Manager - Infectious Diseases




Job Locations

United States-OH-Cincinnati | United States | United States-TX-Irving (Dallas) | United States-CO-Denver | 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 and Project Managers with a focus on Infectious Diseases to join our Clinical Trial Management Group. We have 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
  • 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





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