Clinical Trial Project Manager - Ophthalmology - Dallas

Medpace; Irving (TX); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Flexible work environment

Competitive PTO packages

Employee health and wellness initiatives

Career growth opportunities

Free on-site parking

Discounts on local sports and attractions

Job summary

A leading contract research organization is seeking a Clinical Trial Project Manager specializing in Ophthalmology in Irving, Texas. The candidate will be responsible for overseeing daily operations, ensuring compliance with regulations, and providing cross-functional team leadership. Preferred qualifications include a Bachelor’s degree in a health-related field and 3-5 years of experience as a project manager within a CRO. This role offers a competitive salary and numerous employee benefits.

Qualifications

• 3-5 years as a project/clinical trial manager within a CRO.
• Experience in Phases 1-4; Phases 2-3 preferred.
• Strong management skills for project timelines.

Responsibilities

• Manage day-to-day operations of the project according to defined contracts.
• Serve as primary contact for operational project-specific issues.
• Review and provide input for study protocol and final report.

Skills

Leadership skills

Project management in clinical trials

Knowledge of ICH/GCP regulations

Education

Bachelor’s degree in a health-related field

Advanced degree in a health-related field

Job description

Clinical Trial Project Manager - Ophthalmology

Join to apply for the Clinical Trial Project Manager - Ophthalmology role at Medpace

Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Ophthalmology 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). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Dallas Perks

• Dallas Campus Overview
• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with nonprofit organizations
• Structured career paths with opportunities for professional growth
• Discounts on local sports games, fitness gyms and attractions
• Modern, ecofriendly campus with an on-site fitness center
• Free on-site parking
• Outdoor seating and workspace

Awards

• Named a Top Workplace in 2024 by The Cincinnati Enquirer
• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What To Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.