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Full-time

Clinical Trial Project Manager - Denver, CO

$100K/yr – $190K/yr

Denver, COScience & PharmaceuticalPosted 17d ago

You'll complete your application on the employer's website.

Role overview

Job type

Full-time

Salary

$100K/yr – $190K/yr

Location

Denver, CO

Posted

17 days ago

Job description

Medpace is a contract research organization providing clinical development services to biotechnology, pharmaceutical, and medical device industries. The Clinical Trial Project Manager will oversee day-to-day project operations, serve as the primary Sponsor contact, manage risks and vendors, and provide cross-functional oversight of study teams and deliverables.

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

Preferred

Advanced degree in a health-related field preferred

Phases 2-3 preferred

Advanced degree

Phases 2-3

Benefits

Potential for bonus and equity awards

Medical insurance

Dental insurance

Vision insurance

401(k)

Vacation policy

Sick days

Paid holidays

Work from home flexibility

Short-term disability insurance

Long-term disability insurance

Health savings accounts

Flexible savings accounts

Life and AD&D insurance

Pet insurance

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

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

An interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust

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

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

Company

Full-service clinical research organization for biotech, pharma, and medical devices

Cincinnati, Ohio, USA

http://www.medpace.com/

Founded in 1992

5001-10000 employees

Qualifications

Bachelor's degree in a health-related field

Experience in Phases 1-4

2-5 years as a project/clinical trial manager

Management of overall project timeline

Strong leadership skills

Advanced degree in a health-related field preferred

Phases 2-3 preferred

Required skills

Clinical Trial Management, ICH/GCP, Clinical Trial Phases 1–4, Project Timeline Management, Risk Management, Clinical Research Associate Oversight

Preferred skills

Advanced degree in a health-related field preferred, Phases 2-3 preferred

Experience

2-5 years

Interested in this role?

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