Clinical Trial Project Manager - Infectious Diseases - Denver

Medpace, Inc.
  • Denver, Colorado
  • Full-time
30+ days ago

Job Description

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 at our Denver, CO office. 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;
  • 3-5 years as a project/clinical trial manager within a CRO;
  • Management of overall project timeline; and
  • Strong leadership skills.

Compensation

A target salary range of $100,000 - $190,000 with potential for bonus and equity awards. Your compensation will be based on your skills and experience. Medpace offers the following benefits for full-time positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, pet insurance, and reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations). Applications will be accepted on an ongoing basis. For more details, please discuss with your recruiter.

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 

 

Please note benefits may vary based on country. 

 

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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.

Numbers & Facts

LocationDenver, Colorado
Job TypeFull-time

Skills

  • Biotech and Pharmaceuticalunmatched
  • Cardiologyunmatched
  • Clinical Researchunmatched
  • Clinical Trial Managementunmatched
  • Communication Skillsunmatched
  • Compensation and Benefitsunmatched
  • Contract Research Organization (CRO)unmatched
  • Cross-Functionalunmatched
  • Data Analysisunmatched
  • Drug Developmentunmatched
  • Endocrinologyunmatched
  • GCP (Good Clinical Practices)unmatched
  • ICH Regulationsunmatched
  • Infectious Diseasesunmatched
  • Leadershipunmatched
  • Medical Equipmentunmatched
  • Mentoringunmatched
  • Onboardingunmatched
  • Oncologyunmatched
  • Operations Planningunmatched
  • Patient Careunmatched
  • Project Developmentunmatched
  • Project Planningunmatched
  • Project Trackingunmatched
  • Project/Program Managementunmatched
  • Quality Managementunmatched
  • Regulationsunmatched
  • Research Protocolsunmatched
  • Risk Analysisunmatched
  • Risk Managementunmatched
  • Training Program Developmentunmatched

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