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Supply Chain Advisor (PharmD)

Medpace, Inc.

Cincinnati, OHHybridPosted 1 day ago
Full TimeEntry LevelOperations & Supply ChainCRO
Original posting ↗

Summary

We are seeking a high-caliber Doctor of Pharmacy (PharmD) graduate to join our Clinical Operations team as a Supply Chain Advisor. At Medpace, our pharmacists don't just dispense; they provide critical scientific and operational oversight. In this role, you will leverage your clinical training to serve as the core subject matter expert on the setup, management, and execution of investigational product (IP) supply chains across diverse therapeutic areas like oncology, cardiology, and rare disease. This entry-level role is an exceptional fast-track for a PharmD looking to pivot into the clinical research industry, offering direct exposure to global logistics, protocol analysis, and advanced Interactive Response Technology (IRT).

Job description

Responsibilities

  • Protocol & Supply Chain Advisement: Analyze complex clinical trial protocols from a pharmacy perspective to advise on IP packaging configurations, labeling, blind-maintenance strategies, and optimal site-level storage.
  • Global Setup & Execution: Collaboratively design and implement end-to-end IP supply chain workflows, ensuring strict compliance with global GCP and GMP regulations.
  • IRT System Architecture: Partner with internal teams to set up and enhance Interactive Response Technology (IRT/IXRS) for automated investigator site resupply, patient randomization, and IP dispensation rules.
  • Risk & Excursion Management: Review temperature excursions at clinical sites, evaluate stability data to advise on product viability, and execute corrective and preventive actions (CAPA) to protect patient safety and trial data integrity.

Qualifications

  • Must have a Doctor of Pharmacy (PharmD) degree
  • Ability to escalate
  • Prioritization of daily, weekly, monthly, and project workloads
  • Strong communication and problem-solving skills
  • Ability to effectively collaborate with internal and external colleagues
  • Provides excellent internal and external customer support
  • Understand multiple potential solutions
  • Solid working knowledge of PowerPoint, Excel, Word
  • Understanding of GCP, GMP, GxP is preferred

Requirements

  • Doctor of Pharmacy (PharmD) degree
  • Ability to escalate
  • Prioritization of daily, weekly, monthly, and project workloads
  • Strong communication and problem-solving skills
  • Ability to effectively collaborate with internal and external colleagues
  • Provides excellent internal and external customer support
  • Understand multiple potential solutions
  • Solid working knowledge of PowerPoint, Excel, Word
  • Understanding of GCP, GMP, GxP preferred

Benefits

  • Health Insurance
  • Wellness Benefits
  • Retirement Benefits
  • Paid Time Off
  • On-site Dining Options
  • On-site Fitness Facilities
  • Free Parking

Company overview

Medpace Holdings, Inc. is a global full-service clinical contract research organization (CRO) headquartered in Cincinnati, Ohio, founded in 1992. The company provides comprehensive Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries worldwide. With over 30 years of experience, Medpace employs a scientifically-driven approach that integrates medical, operational, and regulatory expertise across all major therapeutic areas including oncology, cardiology, metabolic diseases, endocrinology, central nervous system disorders, and infectious diseases. The company operates a unique full-service model that includes wholly-owned central laboratories, bioanalytical laboratories, imaging core labs, ECG core labs, and a Phase I clinical unit, all integrated to streamline clinical trial execution. Medpace's global presence spans North America, Europe, Asia Pacific, and Latin America, with approximately 6,000 employees across 44 countries. The company went public in 2016 and trades on NASDAQ under the symbol MEDP, consistently demonstrating strong growth while maintaining its focus on accelerating the development of safe and effective medical therapeutics through high-quality clinical research services.

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