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MedpacePosted 22 days ago

Clinical Research Project Coordinator - Gastrointestinal/GI

Full-time
On-site
Entry level
Competitive
Posted 22 days ago

Medpace is a leading contract research organization providing clinical development services to biotechnology, pharmaceutical, and medical device companies. The Clinical Research Project Coordinator will support day-to-day clinical trial management, coordinate project activities and meetings, maintain reports and timelines, and oversee regulatory filings and study supplies.

Posted
22 days ago
Source
careers.medpace.com
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Engage in clinical trial management on a day to day level
  • Work closely with the project CTM for timely delivery of 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 Life Sciences field
  • Excellent computer, organizational, and time management skills; and

Preferred

  • Research experience preferred
  • Research experience

Required skills

Clinical ResearchClinical Trial ManagementQuality ControlRegulatory Filing

Full job description

Medpace is a leading contract research organization providing clinical development services to biotechnology, pharmaceutical, and medical device companies. The Clinical Research Project Coordinator will support day-to-day clinical trial management, coordinate project activities and meetings, maintain reports and timelines, and oversee regulatory filings and study supplies.

Responsibilities

  • Engage in clinical trial management on a day to day level
  • Work closely with the project CTM for timely delivery of 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 that incorporates a virtual and hands-on learning experience
  • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
  • 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
  • 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
  • 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 and intramural sports
  • Modern corporate campus designed to support collaboration and productivity
  • Multiple on-site dining options in the heart of Madison Square
  • Free on-site parking
  • Convenient access to on-site 24-7 fitness and wellness facilities

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 Life Sciences field
  • Excellent computer, organizational, and time management skills; and
  • Research experience preferred

Required skills

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

Preferred skills

  • Research experience preferred

Experience

  • Entry level

Job details

Employment type

Full-time

Seniority level

Entry level

Date posted

Oct 22, 2026

Work mode

On-site

Job source

careers.medpace.com

Company

Medpace

Healthcare

Full-service clinical research organization for biotech, pharma, and medical devices

See all 19 jobs from Medpace →
  • Cincinnati, Ohio, USA
  • Healthcare
  • 5001-10000 employees
  • Founded 1992
  • medpace.com

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