Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO

Medpace, Inc.•Denver, CO

74d•Onsite

About The Position

Medpace is seeking a full-time, office-based Associate Clinical Trial Manager (aCTM) for its Clinical Trial Management team in Denver, Colorado. The role supports Project Coordinators and Clinical Trial Managers with project management activities. The successful candidate will apply analytical and academic skills to clinical project administration and management. The position offers foundational training and an opportunity to develop toward Clinical Trial Management, with an intensive training period and an accelerated career path for candidates who demonstrate the aptitude and interest. The role is focused on supporting global clinical study activities, maintaining accurate project records and timelines, coordinating meetings, and communicating with internal and external study partners. Medpace is a full-service clinical contract research organization providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries.

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 in the CRO or pharmaceutical industry is advantageous but not required.
PhD and/or post-doctoral research experience related to oncology, hematology, or radiopharmaceuticals.

Responsibilities

Communicate and collaborate on global study activities with the Project Coordinator and Clinical Trial Manager.
Complete recurring tasks consistently and accurately, delivering them on time.
Compile and maintain project-specific status reports in the clinical trial management system.
Interact with internal project teams, sponsors, 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 prepare quality meeting minutes.

Benefits

Medical, dental, and vision insurance.
401(k).
Vacation policy, sick days, and paid holidays.
Work-from-home flexibility; the position is office-based, with occasional work from home potentially available for eligible positions after training.
Short-term and long-term disability insurance.
Health savings and flexible spending accounts.
Life and accidental death and dismemberment insurance.
Pet insurance.
Reimbursement for travel expenses, including food and gas allowance, rental cars, and hotel accommodations.
Company-sponsored social events.
Competitive compensation programs that recognize and reward performance.
On-site mentors, defined career paths, onboarding and training programs, and ongoing learning and development opportunities.