Associate Clinical Trial Manager - PhD - Postdoctoral - CNS/Neuroscience

Medpace; Irving (TX); On-site; USD 70,000 - 110,000; Full time

Job summary

An established industry player is seeking a dedicated Associate Clinical Trial Manager to join their Clinical Trial Management team. This role offers a unique opportunity for recent PhD graduates to transition into the industry, providing extensive training and a clear path for career advancement in the field of clinical trials. You will work closely with project coordinators and clinical trial managers, ensuring the successful execution of clinical studies. This position promises a collaborative environment where your analytical skills will directly contribute to the development of groundbreaking therapeutics.

Benefits

Flexible work environment

Competitive PTO packages

Employee health and wellness initiatives

Discounts on local sports games

Modern, ecofriendly campus

Structured career paths

Discounted tuition for UC online programs

Qualifications

• PhD in Life Sciences required; expertise in CNS/Neuroscience is crucial.
• Ability to work in a fast-paced dynamic industry within an international team.

Responsibilities

• Communicate and collaborate on global study activities.
• Ensure timely delivery of tasks with high accuracy.
• Compile and maintain project-specific status reports.

Skills

CNS/Neuroscience expertise

Analytical skills

Project management

Communication skills

Education

PhD in Life Sciences

Job description

Associate Clinical Trial Manager - PhD - Postdoctoral - CNS/Neuroscience

Job Locations

United States-OH-Cincinnati | United States-TX-Irving (Dallas) | United States-CO-Denver

Category

Clinical Trial Management

Job Summary

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to CNS/Neuroscience for a full-time, office-based Associate Clinical Trial Manager (aCTM). The aCTM is part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities

Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
• Ensure timely delivery of recurrent tasks consistently 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, Sponsor, study sites, and third-party vendors
• Provide oversight and quality control of our 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 CNS/Neuroscience
• Ability to work in a fast-paced dynamic industry within an international team
• Prior experience within the CRO or pharmaceutical industry not required but will be advantageous

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Cincinnati Perks

• Cincinnati Campus Overview
• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with local nonprofit organizations
• Discounts on local sports games, fitness gyms and attractions
• Modern, ecofriendly campus with an on-site fitness center
• Structured career paths with opportunities for professional growth
• Discounted tuition for UC online programs

Awards

• Named a Top Workplace in 2024 by The Cincinnati Enquirer

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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