Clinical Trial Project Manager - Neuroscience - Dallas

Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Project Managers with a focus on Neuroscience or CNS to join our Clinical Trial Management Group in our Dallas, TX office. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.

Responsibilities

Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations

Serve as primary Sponsor contact for operational project-specific issues and study deliverables

Maintain in depth knowledge of protocol, therapeutic area, and indication

Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided

Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable

Develop operational project plans

Manage risk assessment and execution

Responsible for management of study vendor

Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

Qualifications

Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred

Experience in Phases 1-4; Phases 2-3 preferred

3-5 years as a project/clinical trial manager within a CRO;

Management of overall project timeline

Strong leadership 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

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.

Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations

Serve as primary Sponsor contact for operational project-specific issues and study deliverables

Maintain in depth knowledge of protocol, therapeutic area, and indication

Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided

Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable

Develop operational project plans

Manage risk assessment and execution

Responsible for management of study vendor

Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred

Experience in Phases 1-4; Phases 2-3 preferred

3-5 years as a project/clinical trial manager within a CRO;

Management of overall project timeline

Strong leadership skills