Supply Chain Advisor (PharmD)

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).

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;
• Stong 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 Power Point, Excel, Word; and
• Understanding of GCP, GMP, GxP is preferred

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

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• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

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• Contribute to an 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

Continuous Growth & Development

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• 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

Other Employee Benefits

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• 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

Cincinnati Headquarters Experience

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• A 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

What to Expect Next A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

• 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.
• Must have a Doctor of Pharmacy (PharmD) degree;
• Ability to escalate;
• Prioritization of daily, weekly, monthly, and project workloads;
• Stong 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 Power Point, Excel, Word; and
• Understanding of GCP, GMP, GxP is preferred