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Regulatory Research Spring 2025 Intern

0-2 years
Not Disclosed
10 Jan. 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Regulatory Submissions Intern

Location: Cincinnati, OH (Office-Based)
Department: Site Activation and Maintenance (SAM)
Company: Medpace


Job Summary

Join our Regulatory Submissions team as an Intern for the spring 2025 semester! You'll support key start-up activities to ensure clinical trials are initiated efficiently. This hands-on role allows you to assist the Regulatory Submissions Coordinators and Managers in maintaining study timelines, collecting essential documents, and addressing regulatory challenges. Gain valuable training and experience through our Site Activation & Maintenance (SAM) Training Program.


Responsibilities

  • Assist the study start-up team with compliance tasks.
  • Perform quality reviews of trial documents within the Trial Master File (TMF).
  • Participate in the SAM Training Program to develop your skills:
    • Complete independent learning modules and interactive workshops.
    • Work on real-world tasks under the guidance of a mentor.
    • Contribute to efficient and seamless study start-up processes.

Qualifications

  • Education:
    • High School Diploma required.
    • Pursuing a Bachelor’s degree in business or life sciences preferred.
  • Proficient in Microsoft Office.
  • Strong organizational and prioritization skills.
  • Availability:
    • Minimum of 20 hours per week; full-time preferred.
    • Must be available to work in the Cincinnati, OH office.
  • Travel: None.

About Medpace

Medpace is a global clinical contract research organization (CRO), specializing in Phase I-IV clinical development. Headquartered in Cincinnati, Ohio, we employ over 5,000 professionals across 40+ countries. Our mission is to accelerate the development of life-changing medical therapies through science and precision.


Why Medpace?

People. Purpose. Passion.

  • Training & Growth: Comprehensive learning opportunities with structured career paths.
  • Community Impact: Contribute to clinical advancements that improve lives.

Cincinnati Perks

  • Modern Campus: Eco-friendly environment with an on-site fitness center.
  • Community Engagement: Collaborate with local nonprofits and enjoy discounts on attractions.
  • Employee Well-Being: Health initiatives and company-sponsored events.
  • Career Development: Tuition discounts for UC online programs and growth opportunities.

Awards & Recognition

  • Top Workplace: Cincinnati Enquirer, 2024.
  • Forbes: America’s Most Successful Midsize Companies (2021–2024).
  • CRO Leadership Awards: Recognized for expertise, quality, and reliability.

What to Expect Next

After reviewing your application, our team will contact qualified candidates to discuss next steps.

Medpace is an Equal Opportunity Employer, fostering diversity and inclusion.