Senior Manager, Global Supply Chain

What You’ll Do:

The Senior Manager, Global Supply Chain reports to the Associate Director, Global Supply Chain and possesses a strong proficiency in clinical supply management and project management practices. The Senior Manager, Global Supply Chain will support the Associate Director, Global Supply Chain to ensure uninterrupted supply of Investigational Medicinal Product (IMP) for clinical studies as well as inventory of comparator drug products (if applicable). 

 

Required location: Waltham, MA (hub-based, onsite 3-4 days per week)

 

Responsibilities:

• Supporting investigational drug product supply and logistics activities, including, but not limited to, demand forecasting and supply planning, IRT start-up and maintenance, label development and proof generation, packaging and labeling operations, release, distribution, expiry extension, pharmacy manual development, returns, reconciliation, destruction, and inventory management

• Support oversight in monitoring inventory levels throughout the life of a clinical trial

• Supporting oversight of packaging and labeling/distribution vendors, including relationship management

• Interpret clinical synopses and protocols to create clinical IMP demand forecasts

• Attend clinical study and cross functional meetings as needed 

• Support global supply chain lead in overseeing the execution of multiple clinical trials and proactively identify potential supply chain issues, and recommend solutions to global supply chain lead

• Support clinical study close-out activities, including returned goods reconciliation and inventory destruction

• Assist with change controls and deviations as needed 

• Support temperature excursion processes as required

• Support the IRT System Leads as necessary with regards to user requirement specifications and management module(s) as applicable

 

Required Qualifications:

• Experience managing clinical supplies for late phase, global clinical trials 

• 8+ years of relevant biopharmaceutical industry experience with 5+ years in clinical supply management

• Knowledgeable in the implementation and workings of IRT systems

• Ability to create a collaborative environment and manage multiple project activities

• Strong computer skills including MS Office

• Hands-on, roll-up-your-sleeves, collaborative approach with high sense of urgency and drive for results

• Ability to think outside of the box and challenge the status quo

• Desire to work in a fast-paced, innovative environment

 

Education:

• Bachelor’s degree in pharmaceutical science, engineering, life sciences, or another relevant field. Advanced degree preferred