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Responsibilities

  • Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial
  • Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF)
  • Collect, review, organize, and assemble regulatory start-up submissions (including submissions to Institutional Review Boards (IRB)
  • Maintain timelines for study start-up through both internal and external collaboration
  • Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements; and
  • Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges
  • Complete independent learning modules, interactive exercises, and team workshops through the core curriculum
  • Gain exposure to real-world tasks through a robust mentoring program; and
  • Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials

Qualifications

  • Bachelor's degree required
  • 1-5+ years of prior experience as a study coordinator or within the pharmaceutical industry
  • Excellent organization and communication skills
  • Knowledge of Microsoft® Office
  • Travel: None

Preferred

  • preferably in a Life Sciences field
  • study start-up experience preferred

Required skills

Clinical Research CoordinationStudy Start-Up

Full job description

Study Start-Up Coordinator – Clinical Research Coordinator Experience jobs in United States

Medpace

  • Biotechnology

Responsibilities

  • Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial
  • Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF)
  • Collect, review, organize, and assemble regulatory start-up submissions (including submissions to Institutional Review Boards (IRB)
  • Maintain timelines for study start-up through both internal and external collaboration
  • Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements; and
  • Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges
  • Complete independent learning modules, interactive exercises, and team workshops through the core curriculum
  • Gain exposure to real-world tasks through a robust mentoring program; and
  • Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials

Preferred

  • preferably in a Life Sciences field
  • study start-up experience preferred

Benefits

  • 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
  • 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
  • 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

  • Bachelor's degree required
  • 1-5+ years of prior experience as a study coordinator or within the pharmaceutical industry
  • Excellent organization and communication skills
  • Knowledge of Microsoft® Office
  • Travel: None
  • Preferably in a Life Sciences field
  • Study start-up experience preferred

Required skills

  • Clinical Research Coordination, Pharmaceutical Industry Experience, Study Start-Up

Preferred skills

  • preferably in a Life Sciences field, study start-up experience preferred

Experience

  • 1+ years

Job details

Employment type

Full-time

Seniority level

1+ years

Date posted

Oct 21, 2026

Work mode

On-site

Job source

careers.medpace.com

Company

  • Dallas, TX
  • Healthcare

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