Job Description
Job Description
The Associate Director, Clinical Supply Chain Management’s primary responsibility is to manage the clinical supply chain for Phase 1 to Phase IV compounds. The completion of clinical trials is the rate-limiting step for filing of new drug applications and, ultimately, to product commercialization. The on-time initiation, uninterrupted conduct, and completion of clinical studies is dependent on the timely delivery of clinical supplies of top quality to the clinical sites.
Responsibilities
• Define and implement a global clinical supply strategy, including the development of strategic options for the clinical supply chain.
• Ensure all clinical supplies (Phases I-IV, affiliate studies, and IIS) are delivered on time, on budget and of top quality with no studies interrupted or delayed due to clinical supplies
• Define and manage external budget for compounds (comparators, co-meds, over-encapsulation, depots, and importation costs)
• Represent the clinical supply chain on Integrated Evidence Strategy Teams (IESTs) and participate and contribute to Product Presentation and Device Strategy Team (PPDST) meetings
• Define API and drug product requirements and delivery dates to support the clinical supply chain
• Matrix management of a larger number of Clinical Supply Project Managers (CSPMs) supporting the global clinical supply chain
• Allocate bulk drug product to CSPMs, minimizing wastage
• Lead the recovery of clinical supplies during a product recall, support the evaluation and approval of non-medical complaints (NMCs), exception reports and recalls
• Demonstrate leadership skills by driving for continuous improvement and encouraging and supporting collaboration across departments. Represent CDSM Program Management on cross-functional and global initiatives which require clinical drug supply expertise.
Qualifications
• Bachelor’s Degree or higher in Pharmacy or Science.
• 8+ years’ experience in the pharmaceutical industry, preferably with CMC and/or clinical supplies management experience.
• Broad understanding of the overall drug development process.
• Experience in project management, planning, forecasting, budgeting.
• Excellent interpersonal, team, and leadership skills.
• Sound knowledge of GxP.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
💡 Quick Summary
Seeking a career-building opportunity? The Associate Director, Clinical Supply Chain Management position is now open for candidates interested in the Operations Executive Jobs sector. This role in Chicago offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Operations Executive Jobs is a plus.
