Medpace - Cincinnati, OH

posted 4 months ago

Full-time - Entry Level
Remote - Cincinnati, OH
1,001-5,000 employees
Professional, Scientific, and Technical Services

About the position

As a Clinical Supply Chain Project Specialist at Medpace, you will play a crucial role in supporting the Clinical Packaging & Supplies (CP&S) department. This position is designed for PharmD candidates who are eager to apply their pharmaceutical knowledge in a dynamic and impactful environment. You will be responsible for collaborating on all activities related to the investigational supply chain, ensuring that clinical study protocols are effectively translated into actionable supply chain strategies. Your role will involve monitoring the alignment of CP&S timelines with overall project timelines, which is essential for the successful execution of clinical trials. In addition to your core responsibilities, you will participate as a member of the project study team, attending internal meetings as well as teleconferences with sponsors and vendors. This collaborative approach will require you to work closely with the Clinical Trial Manager and the Start-up Label Coordinator to facilitate the development and approval of labels for investigational products. Your ability to communicate effectively and solve problems will be vital as you navigate the complexities of clinical trial management. This position offers a unique opportunity to leverage your PharmD background in a full-service clinical contract research organization (CRO) that is dedicated to accelerating the global development of safe and effective medical therapeutics. Medpace is committed to providing a supportive work environment where you can grow professionally while making a significant impact on patient care.

Responsibilities

  • Support and collaborate in all activities related to investigational supply chain.
  • Translate clinical study protocol into investigational supply chain.
  • Monitor alignment of CP&S timelines with project timelines.
  • Attend internal, Sponsor, and/or Vendor teleconferences as a member of the project study team.
  • Collaborate with Clinical Trial Manager and Start-up Label Coordinator for label development and approval.

Requirements

  • PharmD degree required.
  • Ability to escalate issues as necessary.
  • Strong prioritization skills for daily, weekly, monthly, and project workloads.
  • Good communication and problem-solving skills.
  • Ability to effectively communicate and collaborate with internal and external colleagues.
  • Understanding of multiple potential solutions to problems.
  • Solid working knowledge of PowerPoint, Excel, and Word.
  • Interest in gaining new experiences in Medpace.
  • Understanding of GCP, GMP, GxP is preferred.

Benefits

  • Hybrid work-from-home options (dependent upon position and level)
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Flexible work schedule
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs
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