Clinical Trial Project Manager - Cardiovascular, Renal, Gastrointestinal - Denver

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
• 3-5 years as a project/clinical trial manager within a CRO; Management of overall project timeline
• Strong leadership skills

Pay

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.

Benefits

• 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
• Reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations)

About the Role

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 in our Denver, CO office.

Requirements

We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.

Skills

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Benefits

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Schedule

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