Shawn Foreman

Experience

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  Polaris Laboratories

  Jan 2002 - Oct 2003

  Lab Supervisor

  ▪ Supervised the work of laboratory personnel engaged in performing routine and specialized procedures, including planning laboratory work, evaluating work performed and handling procedural and technical laboratory problems.▪ Responsible for following quality assurance/quality control (QA/QC) procedures for analysis of lubrication samples.▪ Conducted testing on lubrication products in accordance with ASTM test methods utilizing laboratory instrumentation (ICP, Particle Counter, Viscometer, IR, and Titration).▪ Performed maintenance of laboratory equipment. Troubleshoot and diagnosed equipment problems and performed standard repairs. Show less

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  Roche Diagnostics

  Oct 2003 - Nov 2010

  Senior Scientific Specialist

  Manufacture and compound more than 600 diagnostic reagents, calibrators, and controls with focus on Therapeutic Drug Monitoring Reagent systems and Drugs of Abuse Testing Reagent systems.▪ Accountable for the execution of validation protocols for new and existing diagnostic products developed and manufactured by Roche.▪ Key contributor to the successful completion of Roche’s Legacy Validation Project.▪ Key contributor in Validation of Antibody purification process by performing guard band studies of the critical process parameters.▪ Worked closely with IT to author, review, and execute validation documentation for System Testing and User Acceptance Testing.▪ Key contributor in the Computer System Validation by drafting, reviewing, and executing protocols for Installation Qualifications, System Qualification and User Acceptance Testing. Show less

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  Traditions Tree Farm, LLC

  Jan 2011 - Jun 2020

  Co-Owner

  Traditions Tree Farm offers choose-and-cut Christmas tree services for families and individuals in the surrounding area. Creating and providing traditions for families in the community is the main goal of Traditions Tree Farm. This is done by offering quality Christmas trees in a family oriented environment.

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  Fisher Clinical Services

  Feb 2011 - Jun 2014

  Position is responsible for the development and mentoring of members of the Clinical Trial Support Department and to ensure that all Fisher Clinical Services Standard Operating Procedures, CGMPs and business practices, especially in regard to our customers, are adhered to by all direct reports. The New Drug Product (NDP) Trial Support Associate is responsible for managing inventory of drug product that will be used in the packaging of clinical supplies. Additionally, this position is responsible for determining the expiration date of clinical trial material. This position requires the ability to understand the demand for clinical trial material and ensure the timely supply of high-quality clinical trial material.

  • Team Leader Project Manager (NDPTS)

    Oct 2012 - Jun 2014

  • New Drug Product Trial Support Associate

    Feb 2011 - Oct 2012
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  Eli Lilly and Company

  Jun 2014 - Mar 2023

  The CTMMS Planning Organization is accountable for the development of molecule/study demand forecasts in partnership with the clinical team and the subsequent implementation of the supply plans. Additionally the CTMMS Planing organization is accountable for adequate and timely supply of New Drug Product and Finished Goods that ultimately ensures CT Material availability for patients. This will be accomplished by planning and scheduling via a MRP system (SAP).The Molecule Planner is part of the CTMMS Planning Function and is responsible for using SAP to develop supply plans for the molecules/studies they are responsible for. The Molecule Planner partners with the Demand Fore-caster to understand key elements of the molecule/study plans and ensures the supply plan is appropriate to meet all demands and dating requirements for the molecule/study. The Molecule Planner is responsible for creating and maintaining P-reqs and Planned Orders for Each Plant and partnering with the Plant Planners to understand any issues with schedules, yields or delivery issues that may impact the supply plan.The supply plan generated and decisions made by the Molecule Planner have far reaching, global impact. The supply plan drives execution activities across all CTMMS, other external functions, and internal and external manufacturing, packaging, and distribution plants around the globe. The plan also directly impacts global Business Unit budgets and Lilly’s ability to meet Corporate clinical trial milestones. Show less

  • Associate Director - Clinical Trial Supply Management

    Mar 2022 - Mar 2023

  • Consultant- Clinical Trial Supply Manager

    Nov 2019 - Mar 2022

  • Consultant Molecule Planner

    Jun 2015 - Nov 2019

  • Associate Consultant - Clinical Supply Coordinator

    Jun 2014 - Jun 2015
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  Loxo@Lilly

  Mar 2023 - now

  Associate Director Clinical Trial Supply Management