Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Denver

Medpace, Inc.•Denver, CO

74d•Onsite

About The Position

Medpace is seeking a candidate with a PhD and/or postdoctoral research experience related to ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in its Denver, Colorado office. The aCTM is part of the Clinical Trial Management team and works with Project Coordinators and Clinical Trial Managers on clinical trial management activities. The role is suited to someone who wants to apply analytical and academic skills to clinical project administration and management. This opportunity offers recent PhD graduates foundational training, work in an international environment, and a path to develop a career in research and development of therapeutics. The role includes an intensive training period and an accelerated career path toward Clinical Trial Management. Prior CRO or pharmaceutical industry experience is not required, but is advantageous. Medpace is a full-service clinical contract research organization providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. It employs more than 6,500 people across over 40 countries. The position is office-based, with occasional work-from-home flexibility for eligible positions after training.

Requirements

PhD in Life Sciences.
Expertise related to ophthalmology.
Ability to work in a fast-paced, dynamic industry within an international team.
Desire to transfer and apply analytical and academic skills in clinical project administration and management.

Nice To Haves

Prior experience within a CRO or pharmaceutical industry.

Responsibilities

Communicate and collaborate on global study activities, working closely with the Project Coordinator and Clinical Trial Manager.
Ensure timely and accurate completion of recurring tasks.
Compile and maintain project-specific status reports in the clinical trial management system.
Interact with the internal project team, Sponsor, study sites, and third-party vendors.
Provide oversight and quality control of the internal regulatory filing system.
Provide oversight and management of study supplies.
Create and maintain project timelines.
Coordinate project meetings and produce quality meeting minutes.

Benefits

Medical insurance.
Dental insurance.
Vision insurance.
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.
Travel expense reimbursement, including food and gas allowance, rental cars, and hotel accommodations.
Potential bonus and equity awards.
Company-sponsored social events.
On-site mentors.
Industry-renowned onboarding and training programs.
Ongoing training and continuous learning opportunities.