Director of Clinical Trial Management - Denver, CO

Medpace is continuing to add experienced CTM Directors and Sr. Project Managers to join our Clinical Trial Management Group to office in Denver, CO. This position will be responsible for mentoring CTMs as well as overseeing projects and sponsor relationships. Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.

This position is a full-time office-based role in our Denver, CO office, with some work-from-home flexibility following tenure with the company.

Responsibilities

Mentor Clinical Trial Managers, Project Coordinators, and other study team members in the Denver, CO office

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

Manage study vendors where applicable

Manage site quality and monitoring deliverables

Work collaboratively with HR to support recruitment of new staff in Denver office

Serve as an escalation point for Clinical Operations in the Denver office

Implement and support Medpace corporate strategies in Denver office

Organize a cross-functional leadership team to align and support all associates in the Denver office.

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

Management of overall project timeline

Bid defense experience

Strong leadership skills

Compensation

A target salary range of $175,000 - $250,000 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.

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.

Mentor Clinical Trial Managers, Project Coordinators, and other study team members in the Denver, CO office

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

Manage study vendors where applicable

Manage site quality and monitoring deliverables

Work collaboratively with HR to support recruitment of new staff in Denver office

Serve as an escalation point for Clinical Operations in the Denver office

Implement and support Medpace corporate strategies in Denver office

Organize a cross-functional leadership team to align and support all associates in the Denver office.

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

Management of overall project timeline

Bid defense experience

Strong leadership skills

Compensation

A target salary range of $175,000 - $250,000 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.