Senior Manager, Clinical Supply Chain Logistics

Posted Yesterday
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Chicago, IL, USA
In-Office
156K-214K Annually
Senior level
Pharmaceutical
The Role
Lead clinical supply chain logistics to ensure timely, compliant delivery of investigational medicinal products and ancillary supplies worldwide. Build and oversee clinical supply plans, forecast demand from trial protocols, manage inventory/expiry, coordinate packaging/labeling and cold chain logistics, and collaborate with Clinical, Quality, Regulatory, Manufacturing, finance, and external vendors.
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Job Description:

Job Purpose

The Senior Manager, Clinical Supply Chain Logistics, is responsible for the oversight and distribution of all goods in support of the company’s clinical programs and will lead efforts to ensure timely supply of clinical trial materials.  This is a critical leadership role that will bridge the gap between research and commercialization by ensuring investigational medicinal products (IMPs) and ancillary supplies are delivered to clinical trial sites around the world in a safe, accurate, timely, and compliant manner.  A key aspect of this position will be to work closely with the Clinical team to develop an understanding of clinical trial protocols and to translate those into precise forecasting models.  Based upon the demand and forecasting models, this individual is responsible for working internally within PDTO to develop and oversee a clinical supply plan.  This role is critical to setting up a robust clinical supply model to support national and international studies.  This position will lead the process for delivery and develop the optimal levels of inventories across all sites and support packaging and labeling activities.  This role requires a strong ability to collaborate with multiple functions, including Clinical, Regulatory, Quality, Finance, as well as internal functions within PDTO.  Must have experience with the import and export of clinical materials.

Essential Job Functions

  • Accountable for building a clinical supply plan to provide input to manufacturing, labeling, and forecasting supply activities across internal and external stakeholders.
  • Track inventory levels and expiry dating of clinical goods and component inventory across multiple sites.
  • Collaborate with clinical teams and other internal/external stakeholders to develop demand forecasts based on trial protocols and timelines.
  • Coordinate logistics activities across multiple sites and with multiple partners.
  • Plans and oversees packaging and labeling operations both internally and with CMOs as required to support the clinical supply plan.
  • Participate/lead investigations in close collaboration with Quality, as applicable.
  • Identify issues and/or risks with meeting clinical supply requirements and suggest solutions to meet timelines.
  • Continuously evaluate and improve supply chain planning business processes to optimize operations.

Skills and Qualifications

  • Bachelors in Biological Sciences or related fields.
  • Senior Manager must have a minimum of 8 years of industry experience with at least 5 years in a distribution/logistics environment in the healthcare industry.
  • Experience with controlled substances and Hazardous Materials is considered a plus.
  • Expert knowledge of GxP regulations, strong organizational and forecasting skills, and proven vendor and cross-functional team management.
  • Experience with clinical supply chain planning.
  • Experience with cold chain products is strongly preferred.
  • Experience with IRT, clinical asset tracking, working with and without ERP systems.
  • Experience with labeling requirements for domestic and international studies.
  • Experience working closely with Manufacturing, Project Management, functional team leaders, clinical teams, contract manufacturing partners and/or cold chain shippers and logistics providers.
  • Competencies: Strategic Thinking, Problem Solving, Teamwork and Collaboration, Independent Judgement, Professionalism, Written & Verbal Communication skills, Customer Service focus, Attention to Detail, Results-oriented, Focus on High Quality & Accuracy, Adaptability, Organizational Skills, MS Suite

Working Conditions

  • Position may require periodic evening/weekend work, and periodic overnight travel, as necessary to fulfill obligations.
  • This position is located in Xeris’ Chicago office.

The anticipated base salary range for this position is $155,750 - $213,600.

#LI-ONSITE


We are committed to offering competitive compensation. Starting pay is determined based on a variety of factors, including the role, job-related knowledge, skills, experience, education, internal equity, market data, and the location of the role, where applicable.


Xeris Pharmaceuticals, Inc. (the “Company”) is an equal opportunity employer and does not discriminate based on race, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, veteran status, genetics or any other characteristic protected by law. All qualified candidates are given equal opportunity and the Company’s employment selection decisions are based solely on job-related factors. NOTE:  This job description is not intended to be all-inclusive. The employee may be required to perform other related duties as needed to meet the ongoing needs of the Company.

 

The level of the position will be determined based on the selected candidate’s qualifications and experience. Final determination of the actual base salary offered depends on several factors, including but not limited to the candidate’s skills, experience, education, location, and business needs. Employees are eligible for equity or long-term incentive awards, where applicable.  Field Sales role employees are eligible for a quarterly commission structure. Non-Sales role employees are eligible for an annual bonus. The Company also offers a comprehensive benefits package that includes additional elements such as paid time off benefits, various health, vision, and dental insurance options, 401(k) retirement benefits and more for eligible employees. Details about these and other offerings will be provided at the time a conditional offer of employment is made. Candidates are always welcome to inquire about our compensation and benefits package during the interview process. Individuals hired as temporary employees, interns, and preceptors are not eligible for commissions, bonuses, and/or long-term incentive or equity awards.  Eligibility for other benefits will be based on plan documents.


Accessibility & Reasonable Accommodations

If, because of a medical condition or disability, you require a reasonable accommodation or assistance to complete any part of the application process, please send an e-mail to [email protected] and identify the type of accommodation or assistance you are requesting. Please include the job requisition number in your message. Please note if your request is not for this stated purpose, you will not receive a response to your email. Do not include any medical or health information in this email.


Xeris participates in E-Verify.  E-Verify Participation Poster

EEO is the Law EEO is the Law

EEO is the Law Supplement EEO is the Law Supplement

Pay Transparency Nondiscrimination Provision Pay Transparency Nondiscrimination Provision

Skills Required

  • Bachelor's degree in Biological Sciences or related field
  • Minimum 8 years industry experience with at least 5 years in distribution/logistics in the healthcare industry
  • Experience with import and export of clinical materials
  • Expert knowledge of GxP regulations
  • Experience with clinical supply chain planning and forecasting based on trial protocols
  • Experience with labeling requirements for domestic and international studies
  • Experience with IRT, clinical asset tracking systems, and working with and without ERP systems
  • Experience working with cold chain shippers, cold chain products
  • Experience with controlled substances and Hazardous Materials
  • Proven vendor and cross-functional team management, including collaboration with Manufacturing, Project Management, CMOs, and logistics providers
  • Proficiency with MS Suite (Microsoft Office)
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The Company
HQ: Chicago, IL
395 Employees
Year Founded: 2005

What We Do

We're a growth-oriented biopharmaceutical company improving patient lives by developing and commercializing advanced products across a range of therapies.

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