Entry-Level Trial Master File (TMF) Specialist

We are currently hiring entry-level 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 administrators, specialists, and clinical research professionals that can help you grow your skillset while working for a growing and developing company. *This position is office-based in Cincinnati, OH.

Responsibilities

Provide guidance and support to study team members and sponsors regarding TMF management;

Initiate and manage TMF Specifications based on scope of work, protocol, and other core documents working with functional area leads and sponsor contacts;

Set up and maintain study specific TMF folder structure;

Support CTMs with review of TMF Plans as required;

Support study team(s) during periodic TMF QCs by assisting with report development and metric reporting;

Report on TMF Health to Sponsors and CTMs;

Contribute to audit/inspection readiness activities by reviewing the TMF, TMF Specifications, and TMF Plans for accuracy, consistency, and completeness;

Train and mentor other TMF staff; and

help with other project and responsibilities, as assigned.

Qualifications

Bachelor's degree, life science field preferred

Proficient knowledge of Microsoft® Office and Adobe Acrobat®

Computer literacy (i.e., ability to file, scan, create folders, and organize files using various

software);

Ability to accurately and carefully follow procedures for completing work tasks; and

Ability to perform repetitive work without losing effectiveness/accuracy.

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

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Provide guidance and support to study team members and sponsors regarding TMF management;

Initiate and manage TMF Specifications based on scope of work, protocol, and other core documents working with functional area leads and sponsor contacts;

Set up and maintain study specific TMF folder structure;

Support CTMs with review of TMF Plans as required;

Support study team(s) during periodic TMF QCs by assisting with report development and metric reporting;

Report on TMF Health to Sponsors and CTMs;

Contribute to audit/inspection readiness activities by reviewing the TMF, TMF Specifications, and TMF Plans for accuracy, consistency, and completeness;

Train and mentor other TMF staff; and

help with other project and responsibilities, as assigned.

Bachelor's degree, life science field preferred

Proficient knowledge of Microsoft® Office and Adobe Acrobat®

Computer literacy (i.e., ability to file, scan, create folders, and organize files using various

software);

Ability to accurately and carefully follow procedures for completing work tasks; and

Ability to perform repetitive work without losing effectiveness/accuracy.