Manager, Clinical Drug Supply & Logistics

Regeneron; Armonk (NY); On-site; USD 113,000 - 185,000; Full time

Job summary

A leading biotechnology company in Armonk is seeking a Manager for Clinical Drug Supply & Logistics. This role entails overseeing supply chain operations for clinical trials, ensuring timely and compliant distribution, and improving processes within a collaborative team environment. Ideal candidates have robust supply chain knowledge with at least 5 years of life science experience.

Benefits

Health and wellness programs

Fitness centers

Equity awards

Annual bonuses

Paid time off

Qualifications

• 5+ years of life science experience.
• 4 years of clinical supply management.
• Knowledge in supply chain and logistics.

Responsibilities

• Manage supply planning for clinical trials.
• Forecast IP supply requirements for clinical studies.
• Oversee IP inventory strategy and shipment orders.

Skills

Supply chain management

Forecasting

Collaboration

Communication

Tools

Interactive Response Technologies (IRT)

Job description

Manager, Clinical Drug Supply & Logistics

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Manager, Clinical Drug Supply & Logistics

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The Manager, Clinical Drug Supply & Logistics is responsible for forecasting Investigational Product (IP) supply requirements for multiple clinical trials and for managing the IP distribution process to one or more clinical trials. Activities are performed on time, within budget and with good quality, in compliance with Regulatory Authorities’ regulations / guidelines and Regeneron SOPs / WPDs. Contributes to ongoing process improvement initiatives. This role applies to internally sourced studies and/or CRO/Partnered studies. Collaborates and interacts with clinical trial managers, development program managers, medical monitors, as well as staff from quality, clinical compliance, regulatory, formulations, and IOPS (CMC, external manufacturing, stability).

A Typical Day Includes

• Serves as lead drug supply manager of multiple small and/or less complex clinical studies for the functional area in supply planning, including demand forecasting according to IOPS requirements.
• Manages supply planning and timelines to ensure alignment with study plans and timelines and overall clinical development plan.
• Manages and oversees investigational product (IP) inventory strategy; advises supply management team of potential shortages and defines resupply activities based on usage trends and projections.
• Oversees IP shipment orders according to supply plans or as requested by Clinical Trial Management team, to ensure timely and compliant shipment and delivery to investigator sites. Works with Clinical Logistics Associate to complete this activity and/or manages any/all aspects of the process.
• Working knowledge and experience with Interactive Response Technologies (IRT) such as IVRS and IWRS.
  
  

This Job May Be For You If

• You are a strong collaborator and can effectively communicate globally
• You are able to work in ambiguous environments
• You have a robust amount of knowledge in supply chain and able to forecast logistical matters
  
  

To be considered, we are looking for you to have 5+ years of Life Science experience and 4 years of clinical supply management. Lastly, we expect you to be onsite a few days a week in one of our offices.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (annually)

$113,100.00 - $184,700.00

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Health Care Provider

• Industries

  Biotechnology

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