Clinical Research Documentation Administrator (TMF)

Medpace, Inc.

Cincinnati (OH)

On-site

USD 42,000 - 56,000

Full time

14 days+

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Benefits offered by this job

Competitive compensation
Health and retirement benefits
Occasional WFH after training
Social events and team sports

Job summary

Medpace, headquartered in Cincinnati, OH, is seeking an organized TMF administrator to manage electronic filing and document control for clinical trials. This role is fully office-based in Cincinnati, OH, requiring strong communication with global teams and meticulous attention to quality control.

You will prepare and ship trial documents, coordinate with departments, and contribute to data integrity across TMF processes while supporting a growing CRO environment.

Qualifications

  • Associates degree, or equivalent required.
  • Bachelor's degree preferred.
  • Some experience in document administration.
  • High attention to detail.
  • Excellent organizational skills.
  • Strong written and verbal communication skills.
  • Knowledge of MS Office.

Responsibilities

  • Manage electronic filing system for trial documentation.
  • Track, maintain, and perform quality check of electronic documents.
  • Communicate with internal associates globally regarding errors in trial documents.
  • Prepare documents for shipment.

Skills

Attention to detail
Organizational skills
Written and verbal communication
Document administration

Education

Associates degree or equivalent
Bachelor's degree preferred

Tools

MS Office

Job description

We are currently hiring individuals seeking an exciting career in clinical research, managing our Trial Master File. The Trial Master File (TMF) is a collection of documents that stores all data and research collected on a given trial. The TMF allows us to conduct a clinical trial and ensures data integrity. It is an integral tool and helps teams manage trials more effectively. TMF oversight is important to the successful execution of a trial and ultimately plays a big role in a new drug or device receiving approval by the FDA. In this position, you will be working with a highly experienced team of other administrators and clinical research professionals that can help you grow your skillset while working for a growing and developing company. *This position is fully office-based in Cincinnati, OH.*

Responsibilities
  • Manage electronic filing system for trial documentation;
  • Track, maintain, and perform quality check of electronic documents;
  • Communicate with internal associates globally regarding errors in trial documents; and
  • Prepare documents for shipment.
Qualifications
  • Associates degree, or equivalent required;
  • Bachelor's degree preferred;
  • Some experience in document administration;
  • High attention to detail;
  • Excellent organizational skills
  • Strong written and verbal communication skills; and
  • Knowledge of MS Office.
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
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Trial Master File Specialist
Trial Master File Specialist

Medpace, Inc. • Cincinnati (OH)

On-site
USD 60,000 - 75,000
Competitive compensation
Health, wellness, retirement, and PTO
On-site dining
+1
Entry-Level TMF Operations Associate
Entry-Level TMF Operations Associate

Medpace, Inc. • Cincinnati (OH)

On-site
USD 40,000 - 52,000
Entry-Level Trial Master File (TMF) Specialist
Entry-Level Trial Master File (TMF) Specialist

Medpace, Inc. • Cincinnati (OH)

On-site
USD 38,000 - 58,000
Associate Clinical Trial Manager - PhD - Metabolic - Cincinnati
Associate Clinical Trial Manager - PhD - Metabolic - Cincinnati

Medpace, Inc. • Cincinnati (OH)

On-site
USD 75,000 - 95,000
On-site mentoring
Career development programs
Competitive compensation
Associate Clinical Trial Manager - PhD - Immunology - Cincinnati
Associate Clinical Trial Manager - PhD - Immunology - Cincinnati

Medpace, Inc. • Cincinnati (OH)

On-site
USD 85,000 - 130,000
Competitive compensation
Health, retirement, and PTO benefits
WFH after training
+1
Associate Clinical Trial Manager: Path to CTM Growth
Associate Clinical Trial Manager: Path to CTM Growth

Medpace • Cincinnati (OH)

On-site
USD 90,000 - 130,000
Flexible work environment
PTO 20+ days
Competitive compensation
+6
Associate Clinical Trial Manager - PhD - Postdoctoral - CNS/Neuroscience - Cincinnati
Associate Clinical Trial Manager - PhD - Postdoctoral - CNS/Neuroscience - Cincinnati

Medpace • Cincinnati (OH)

On-site
USD 70,000 - 90,000
Clinical Data Intern - Spring 2026
Clinical Data Intern - Spring 2026

Medpace • Cincinnati (OH)

Hybrid
USD 15,000 - 21,000
Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology, Renal - Cincinnati
Associate Clinical Trial Manager - PhD - Postdoctoral - Nephrology, Renal - Cincinnati

Medpace, Inc. • Cincinnati (OH)

On-site
USD 65,000 - 90,000
Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Cincinnati
Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Cincinnati

Medpace, Inc. • Cincinnati (OH)

On-site
USD 85,000 - 120,000