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Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO
full-timeDenver$70k - $90k

Summary

Location

Denver

Salary

$70k - $90k

Type

full-time

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About this role

Job Summary

Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Oncology, Hematology, and Radiopharm for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Denver, CO office.  The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project 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; and
  • Coordinate project meetings and produce quality minutes.

Qualifications

  • PhD in Life Sciences;
  • Fluency in English with solid presentation skills;
  • 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; and
  • Excellent computer (word-processing, databases, Excel, Windows), organisational, and communication skills.

Compensation

A target salary range of $70,000 - $90,000 with potential for bonus and equity awards. Your compensation will be based on your skills and experience. Medpace offers the following benefits for full-time positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, pet insurance, and reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations). Applications will be accepted on an ongoing basis. For more details, please discuss with your recruiter.


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.

 

Denver Perks

  • Denver Office 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
  • Structured career paths with opportunities for professional growth
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • RTD Eco Pass
  • Secure bike storage room

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

TWP 2024          CRO2024

 

What to Expect Next

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

Other facts

Tech stack
Project Management,Communication,Collaboration,Analytical Skills,Organizational Skills,Presentation Skills,Quality Control,Regulatory Filing,Timeline Management,Meeting Coordination,Team Interaction,Status Reporting,Computer Skills,Fast-Paced Work,International Teamwork,Clinical Trial Management

About Medpace, Inc.

Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,000 people across 44 countries.

Team size: 5,001-10,000 employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing
Founding Year: 1992

What you'll do

  • The Associate Clinical Trial Manager will support Project Coordinators and Clinical Trial Managers in project management activities, ensuring timely delivery of tasks and maintaining project-specific status reports. They will also interact with internal teams, sponsors, study sites, and vendors while overseeing regulatory filings and study supplies.

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Frequently Asked Questions

What does Medpace, Inc. pay for a Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO?

Medpace, Inc. offers a competitive compensation package for the Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO role. The salary range is USD 70k - 90k per year. Apply through Clera to learn more about the full compensation details.

What does a Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO do at Medpace, Inc.?

As a Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO at Medpace, Inc., you will: the Associate Clinical Trial Manager will support Project Coordinators and Clinical Trial Managers in project management activities, ensuring timely delivery of tasks and maintaining project-specific status reports. They will also interact with internal teams, sponsors, study sites, and vendors while overseeing regulatory filings and study supplies..

Why join Medpace, Inc. as a Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO?

Medpace, Inc. is a leading Pharmaceutical Manufacturing company. The Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO role offers competitive compensation.

Is the Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO position at Medpace, Inc. remote?

The Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO position at Medpace, Inc. is based in Denver, Colorado, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO position at Medpace, Inc.?

You can apply for the Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Denver. CO position at Medpace, Inc. directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Medpace, Inc. on their website.