Dallas Clinical Research Project Coordinator

Medpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology and more. If you are looking for a fast paced, collaborative work environment in clinical research and want to develop your career even further, then this is the opportunity for you. Medpace provides Project Coordinators a 4-6 week training program that incorporates a virtual and hands on learning experience, especially for those without previous clinical research experience.

Responsibilities

Engage in clinical trial management on a day to day level;

Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;

Compile and maintain project-specific status reports;

Interact with the Sponsor, study sites, and internal associates;

Provide oversight and quality control of our internal regulatory filing system;

Manage study supplies;

Create and maintain project timelines; and

Coordinate project meetings and produce quality meeting minutes.

Qualifications

Minimum of a Bachelor’s Degree in a Life Sciences field;

Excellent computer, organizational, and time management skills; and

Research experience preferred.

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

Please note benefits may vary based on country.

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.

Engage in clinical trial management on a day to day level;

Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;

Compile and maintain project-specific status reports;

Interact with the Sponsor, study sites, and internal associates;

Provide oversight and quality control of our internal regulatory filing system;

Manage study supplies;

Create and maintain project timelines; and

Coordinate project meetings and produce quality meeting minutes.

Minimum of a Bachelor’s Degree in a Life Sciences field;

Excellent computer, organizational, and time management skills; and

Research experience preferred.