Manager, Clinical Supply & Logistics (Chicago Based)

Xeris Pharmaceuticals•Chicago, IL

19d•$95,000 - $180,000•Hybrid

About The Position

The Manager, Clinical Supply and Logistics will be the liaison between the Clinical Research Operations team and the Technical Operations team to facilitate cross functional collaboration for proactive problem solving and alignment of end-to-end clinical supply chain management to support clinical trial execution. This position will be responsible for supporting the strategic planning and execution of new clinical trial supply chains on time and within budget and is tasked with supporting an integrated operating model with close collaboration with cross functional stakeholders.

Requirements

Bachelor’s degree (B.A./B.S.) or equivalent, preferably in life sciences or related discipline.
5+ years of related experience supporting clinical trial teams.
Experience managing clinical trial vendors.
A high level of proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook) is also required
Competencies : Teamwork & Collaboration, Attention to Detail, Analytical skills, Organizational skills, Written and Verbal Communications, Adaptability, Time Management skills

Responsibilities

Oversees clinical supply labeling, packaging, release, distribution, return and destruction at contract manufacturing organizations.
Manages inventory globally at depots and sites including order management and proof of delivery confirmation, return or destruction and distribution logistics.
Acts as a key interface between the Technical Operations and Clinical Research Operations teams to operationalize supply strategy to maximize supply efficiency, minimize waste while identifying risk and develop risk mitigation plans.
Interprets protocol or study overview to calculate total demand and translation of total demand into a demand forecast over time.
Manages clinical supply activities for clinical trials including clinical supply needs identification, determination of appropriate presentation to clinical site and participants and IP expiry date management.
Collaborates with project team members including Technical Operations, Regulatory and Quality to design and implement drug labelling, packaging and supply strategies that not only meet the requirements of the study design, the clinical study sites, project timeline and the relevant regulatory authorities, but also maximizes efficiency of supply.
Leads the logistics of the forecasting, planning, and distribution of ancillary supplies for all clinical trials in conjunction with senior team members.
Coordinates supply strategies with internal Supply Chain/Technical Operations team and external packaging suppliers in conjunction with senior team members.
Manages external clinical vendors including IRT vendors, as assigned, in conjunction with senior team members.
Proactively identifies, prevents, and mitigates cross functional program risks related to clinical supply logistics.
Work with the cross functional project team to ensure consistent communication of clinical trial material supply chain status.
Collaborates with cross-functional study team members to ensure compliance of department/study activities with ICH guidelines, GxP, FDA and other applicable country regulations.
Other tasks as requested by managers.