Laboratory Project Coordinator

Medpace Reference Laboratories (MRL) is currently seeking a full-time Project Coordinator. MRL is a full service central clinical trial laboratory offering project management, laboratory services, data management, logistics, and sample management and archiving capabilities, and quality assurance.

Responsibilities

Create and maintain laboratory manuals (general and study-specific) and other study- related documents;

Develop and present clinical laboratory presentations at investigator meetings;

Design specifications and monitor production of specimen collection kits;

Track study status as appropriate;

Communicate all aspects of protocol to various internal departments for appropriate study setup, maintenance, and closeout; and

Write, establish, and revise relevant Standard Operating Procedures and/or work instructions.

Qualifications

Bachelor's degree in science or a health-related field;

Laboratory experience preferred;

Excellent oral and written communication skills.

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.

Create and maintain laboratory manuals (general and study-specific) and other study- related documents;

Develop and present clinical laboratory presentations at investigator meetings;

Design specifications and monitor production of specimen collection kits;

Track study status as appropriate;

Communicate all aspects of protocol to various internal departments for appropriate study setup, maintenance, and closeout; and

Write, establish, and revise relevant Standard Operating Procedures and/or work instructions.

Bachelor's degree in science or a health-related field;

Laboratory experience preferred;

Excellent oral and written communication skills.