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MedpacePosted 25 days ago

Clinical Research Project Coordinator - Infectious Disease

Full-time
On-site
Entry level
Competitive
Posted 25 days ago

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

Posted
25 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

Preferred

  • Research experience preferred

Required skills

Clinical Trial ManagementProject Timeline ManagementRegulatory Filing System

Full job description

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

Benefits

  • 4-6 week training program that incorporates a virtual and hands on learning experience
  • 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
  • Free on-site parking
  • Convenient access to on-site 24-7 fitness and wellness facilities
  • Multiple on-site dining options
  • Glassdoor
  • 3.0
  • Medpace, Inc., a clinical research organization, provides clinical development services for pharmaceutical and biotechnology.
  • Cincinnati, Ohio, USA
  • http://www.medpace.com
  • Public Company
  • Total Funding
  • unknown
  • 2016-08-10
  • IPO
  • 2014-02-24
  • Acquired
  • Leadership Team
  • Kevin M. Brady
  • Chief Financial Officer
  • Brandon Ebken
  • Chief Information Officer
  • Recent News
  • BioSpace
  • Medpace Holdings, Inc. Reports Third Quarter 2026 Results
  • 2026-10-22
  • PR Newswire
  • Kuehn Law Encourages Investors of Medpace Holdings, Inc. to Contact Law Firm

Qualifications

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

Required skills

  • Clinical Trial Management, Project Timeline Management, Regulatory Filing System, Research Experience

Preferred skills

  • Research experience preferred

Experience

  • Entry level

Job details

Employment type

Full-time

Seniority level

Entry level

Date posted

Oct 19, 2026

Work mode

On-site

Job source

careers.medpace.com

Company

  • Cincinnati, OH
  • Healthcare

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