Clinical Trials Project Coordinator - Fast-Paced, Impactful

Medpace; Irving (TX); On-site; USD 50,000 - 65,000; Full time

Benefits offered by this job

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

Job summary

A leading CRO is seeking a full-time Project Coordinator to join the Clinical Trial Management team in Irving, Texas. The role involves engaging in clinical trial management, interacting with sponsors and study sites, and overseeing project timelines. Ideal candidates should hold a Bachelor's degree in a Life Sciences field and possess excellent organizational and time management skills. This position offers a supportive environment for those looking to grow their careers in clinical research with competitive benefits.

Qualifications

• Minimum of a Bachelor’s Degree in a Life Sciences field.
• Excellent computer, organizational, and time management skills.
• Research experience preferred.

Responsibilities

• Engage in clinical trial management on a day to day level.
• Work closely with the project CTM for timely delivery of tasks.
• 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.
• Coordinate project meetings and produce quality meeting minutes.

Skills

Excellent computer skills

Organizational skills

Time management skills

Education

Bachelor’s Degree in a Life Sciences field

Job description

A leading CRO is seeking a full-time Project Coordinator to join the Clinical Trial Management team in Irving, Texas. The role involves engaging in clinical trial management, interacting with sponsors and study sites, and overseeing project timelines. Ideal candidates should hold a Bachelor's degree in a Life Sciences field and possess excellent organizational and time management skills. This position offers a supportive environment for those looking to grow their careers in clinical research with competitive benefits.