Associate Clinical Trial Manager - PhD / Post-Doc Experience - Denver, CO

Medpace, Inc.•Denver, CO

114d•Onsite

About The Position

Medpace is seeking a full-time, office-based Associate Clinical Trial Manager (aCTM) to join its Clinical Trial Management team in Denver, Colorado. The role supports Project Coordinators and Clinical Trial Managers with project management activities and is suited to candidates with a PhD and/or postdoctoral research experience who want to apply their analytical and academic skills to clinical project administration and management. Candidates should expect intensive training and demonstrate the aptitude and interest to pursue an accelerated career path into Clinical Trial Management. The position offers foundational training, an international working environment, and opportunities to develop a career in research and development of therapeutics. Medpace is a full-service clinical contract research organization providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries. It employs more than 6,500 people across more than 40 countries. Its mission is to accelerate global development of safe and effective medical therapeutics through clinical research.

Requirements

PhD in Life Sciences.
Fluency in English and solid presentation skills.
Ability to work in a fast-paced, dynamic industry within an international team.
Excellent computer skills, including word processing, databases, Excel, and Windows.
Excellent organizational and communication skills.

Nice To Haves

Prior experience within a CRO or pharmaceutical industry is advantageous but not required.
Postdoctoral research experience is sought alongside PhD experience.

Responsibilities

Communicate and collaborate on global study activities, working closely with the Project Coordinator and Clinical Trial Manager.
Deliver recurring tasks on time and consistently with a high degree of accuracy.
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

Target salary range of $70,000–$90,000, with potential for bonus and equity awards.
Medical, dental, and vision benefits.
401(k).
Vacation policy, sick days, and paid holidays.
Work-from-home flexibility, including occasional work from home for eligible positions after training.
Short-term and long-term disability insurance.
Health savings and flexible spending accounts.
Life and AD&D insurance.
Pet insurance.
Reimbursement for travel expenses, including food and gas allowance, rental cars, and hotel accommodations.
Competitive compensation programs that recognize and reward performance.
Comprehensive health, wellness, retirement, and PTO benefits.
Company-sponsored social events.
On-site mentors.
Defined career paths with advancement opportunities.
Onboarding, training, and ongoing professional development opportunities.