Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Cincinnati

Medpace

Cincinnati (OH)

On-site

USD 85,000 - 110,000

Full time

14 days+

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Benefits offered by this job

Competitive compensation
Comprehensive health benefits
Office-based with occasional WFH after
Training and onboarding
Team events

Job summary

Medpace is seeking candidates with PhDs and/or Post-Doctoral Research in Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM) in Cincinnati, OH. The aCTM will join the Clinical Trial Management team, collaborating with Project Coordinators and Clinical Trial Managers to manage clinical trial activities and ensure timely, accurate delivery.

This represents a strong entry path for recent PhD graduates to enter industry, with comprehensive onboarding, international

Qualifications

  • PhD in Life Sciences.
  • Ophthalmology expertise.
  • Ability to work in a fast-paced dynamic industry within an international team.
  • CRO or pharma experience not required but advantageous.

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.

Skills

Communication
Team collaboration
Analytical thinking

Education

PhD in Life Sciences
Post-Doctoral Research experience
Ophthalmology expertise

Job description

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmologyfor a full-time, office-based Associate Clinical Trial Manager (aCTM) position in our Cincinnati, OH office. 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 Ophthalmology
  • 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) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work
  • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
  • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
  • Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
  • Office based environment with on-site mentors
  • Defined career paths with clear advancement opportunities
  • Industry renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
  • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office based culture with occasional WFH that provides flexibility for eligible positions after training
  • Company-sponsored social events and intramural sports
Cincinnati Headquarters Experience
  • A modern corporate campus designed to support collaboration and productivity
  • Multiple on-site dining options in the heart of Madison Square
  • Free on-site parking
  • Convenient access to on-site 24-7 fitness and wellness facilities
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