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Associate Clinical Trial Manager - Phd - Metabolic - Dallas, Tx

0-2 years
Not Disclosed
10 Oct. 30, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Clinical Trial Manager – PhD (Metabolic Research)

📍 Location: Irving (Dallas), Texas
📂 Department: Clinical Trial Management
🆔 Job ID: 11684
🏢 Company: Medpace


🔍 Job Summary

Medpace, a leading Contract Research Organization (CRO) for biotech companies, is seeking PhD or Post-Doctoral candidates specializing in Metabolic Research for a full-time, office-based Associate Clinical Trial Manager (aCTM) position.

This role supports the Clinical Trial Management team by assisting Project Coordinators and Clinical Trial Managers in managing and administering clinical projects within metabolic trials.

It’s an excellent opportunity for recent PhD graduates to:

  • Transition into the clinical research industry,

  • Receive structured, foundational training,

  • Work in an international, cross-functional environment, and

  • Build a fast-track career toward Clinical Trial Management (CTM).


🧩 Key Responsibilities

  • Collaborate globally with Project Coordinators and Clinical Trial Managers on study activities.

  • Ensure timely and accurate completion of recurrent project tasks.

  • Compile and maintain project-specific status reports in the Clinical Trial Management System (CTMS).

  • Communicate effectively with internal teams, sponsors, study sites, and third-party vendors.

  • Oversee and maintain the internal regulatory filing system.

  • Manage study supplies and ensure quality control.

  • Create and maintain detailed project timelines.

  • Coordinate project meetings and prepare high-quality meeting minutes.


🎓 Qualifications

  • PhD in Life Sciences (Metabolic research preferred).

  • Fluent in English with strong presentation and communication skills.

  • Ability to thrive in a fast-paced, global environment.

  • Prior CRO or pharmaceutical experience is advantageous but not required.

  • Strong proficiency in MS Word, Excel, databases, and general computer applications.

  • Excellent organizational and interpersonal skills.


🏢 About Medpace

Medpace is a full-service, global CRO providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries.

Mission: To accelerate the global development of safe and effective therapeutics through scientific excellence and operational discipline.

Therapeutic Expertise Includes:

  • Oncology

  • Cardiology

  • Metabolic & Endocrinology

  • CNS (Central Nervous System)

  • Anti-viral and Anti-infective diseases

Headquarters: Cincinnati, Ohio
Global Presence: 40+ countries
Team Size: 5,000+ professionals


🏆 Awards & Recognition

  • Top Workplace 2024The Cincinnati Enquirer

  • Forbes America’s Most Successful Midsize Companies – 2021, 2022, 2023, 2024

  • CRO Leadership AwardsLife Science Leader Magazine (expertise, quality, reliability, compatibility)


💡 Why Join Medpace?

People. Purpose. Passion.
At Medpace, your work will:

  • Directly impact the lives of patients and families,

  • Contribute to advancing global healthcare, and

  • Offer growth within a respected, mission-driven organization.


📩 Next Steps

A Medpace recruitment team member will review your qualifications.
If shortlisted, you will be contacted regarding the next steps in the hiring process.


📤 Apply / Share

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