Dallas Clinical Research Project Coordinator

Medpace is a clinical contract research organization providing clinical development services to biotechnology, pharmaceutical, and medical device companies. The Project Coordinator supports day-to-day clinical trial management by coordinating project tasks, maintaining status reports and timelines, managing study supplies, overseeing regulatory filings, and facilitating communication and meetings among sponsors, study sites, and internal teams.

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

Preferred

• Research experience preferred
• Research experience

Benefits

• 4-6 week training program incorporating a virtual and hands-on learning experience
• 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
• 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

Company

• Full-service clinical research organization for biotech, pharma, and medical devices
• Cincinnati, Ohio, USA
• http://www.medpace.com/
• Founded in 1992
• 5001-10000 employees

Qualifications

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

Required skills

• Clinical Research, Clinical Trial Management, Project Coordination, Quality Control, Regulatory Filing

Preferred skills

• Research experience preferred

Experience

• Entry level