Associate Clinical Trial Manager - PhD - Cardiovascular - Denver

Medpace

Denver (CO)

On-site

USD 70,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Flexible work environment

Competitive PTO starting at 20+ days

Health and wellness initiatives

Modern, eco-friendly campus with on-site fitness center

Job summary

A leading clinical research organization in Denver is seeking an Associate Clinical Trial Manager with a PhD and cardiology experience. This full-time office-based role involves managing project activities, ensuring accuracy in tasks, and maintaining project status reports. Candidates should have a PhD in Life Sciences and a strong background in cardiomyopathy or related fields. The position offers a target salary range of $70,000 – $90,000, along with benefits like flexible work arrangements, PTO, and wellness initiatives.

Qualifications

PhD or post-doctoral researchers with cardiology experience.
Prior CRO or pharmaceutical industry experience is a plus.

Responsibilities

Communicate and collaborate on global study activities.
Ensure timely delivery of recurrent tasks with a high degree of accuracy.
Compile and maintain project-specific status reports.
Interact with internal project teams and third-party vendors.
Provide oversight of internal regulatory filing system.
Create and maintain project timelines.

Skills

Ability to work in a fast-paced dynamic industry

Expertise in cardiomyopathy, lipid disorders, etc.

Education

PhD in Life Sciences

Job description

Associate Clinical Trial Manager – PhD – Cardiovascular

Join the Medpace team as an Associate Clinical Trial Manager – PhD – Cardiovascular in our Denver, CO office. This is a full‑time, office‑based role for PhDs or post‑doctoral researchers with cardiology experience.

Job Summary

Medpace is looking for a candidate who can transfer analytical and academic skills into clinical project administration and management. This position offers intensive training, a clear path to accelerated career progression, and an opportunity to contribute to cutting‑edge therapeutics in an international environment.

Responsibilities

Communicate and collaborate on global study activities; work closely with project coordinators and clinical trial managers.
Ensure timely delivery of recurrent tasks with a high degree of accuracy.
Compile and maintain project‑specific status reports within the clinical trial management system.
Interact with the internal project team, 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 produce quality minutes.

Qualifications

PhD in Life Sciences.
Expertise related to cardiomyopathy, lipid disorders, obesity, heart failure, endocrinology, NASH, acute coronary syndrome, CVD, or preventive cardiology.
Ability to work in a fast‑paced dynamic industry within an international team.
Prior CRO or pharmaceutical industry experience is a plus.

Compensation & Benefits

Target salary range: $70,000 – $90,000, with potential for bonus and equity awards. Full‑time benefits include medical, dental, vision, 401(k), vacation, sick days, paid holidays, work‑from‑home flexibility, short‑term and long‑term disability, health savings account, flexible savings account, life and AD&D insurance, pet insurance, and travel expense reimbursement.

Medpace Overview

Medpace is a full‑service clinical contract research organization (CRO) providing Phase I‑IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, we employ more than 5,000 people across 40+ countries.

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