Skip to main content

Clinical Supply Chain Manager

Aplica ya
Mapa de ubicación: Plymouth Meeting, Pennsylvania, United States Full time R1251116

Descripción del trabajo

Job Overview
The Senior Clinical Supply Chain Manager is responsible for  managing the strategic planning and execution of a program of assigned clinical supply chain projects. The Senior Clinical Supply Chain Manager will support the ongoing development and optimization of the Clinical Trial Supplies department and processes for our preferred sponsor.

Essential Functions

  • Manage clinical supply planning and forecasting for study protocols, with focus on less complex study designs

  • Serve as member of clinical study team and/or clinical drug supply team, as assigned

  • Interpret relevant protocol information to develop packaging/labeling design and/or global distribution strategy

  • Coordinate the origination, proofing and translation of clinical study labels, as required

  • Support design and set-up of IVRS system

  • Support financial planning for global clinical supplies, including budgeting, forecasting, and strategic planning activities for clinical trials and pharmaceutical development pipeline

  • Manage drug supply delivery timelines with Clinical, packaging source area(s), and indirectly with GMP laboratories, QA and Regulatory Affairs, as required

  • Prepare required documentation and assist internal and external stakeholders to facilitate activities for the import and export of clinical supplies, as required.

  • Maintain close communications with all internal-chain groups to ensure the adequate supply of clinical supplies throughout the duration of a clinical trial

  • Monitor global clinical supply inventory for both IVRS and traditional studies via tracking of specific milestone dates and adjusting drug distribution plan accordingly

  • Resolve issues involving distribution of clinical supplies, including US & International shipments, temperature excursions, etc.

  • Manage clinical supply complaints received from investigative sites and/or subsidiaries, address supply replacement requests. 

  • Monitor expiry dating for clinical study supplies.  

  • Interact with other departments, as needed, to resolve any issues involving clinical supply inventory and distribution. 

  • Ensure that all tasks meet Sponsor and PRA expectations, and are delivered in accordance with the contract, trial protocol, ICH/GCP and applicable SOPs.


  • Bachelor's Degree in health sciences or related field

  • Minimum of 3-5 years of relevant work experience

  • Prior experience in pharmaceutical, biotech, and clinical supply logistics is preferred

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities.  Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at to arrange for such an accommodation.

Aplica ya

Únase a la red de talentos de IQVIA

Regístrese hoy y le informaremos cuando haya puestos disponibles que coincidan con sus intereses profesionales.

Únase a nuestra red
Top of page