Company:Array BioPharma is a biopharmaceutical company headquartered in Boulder, Colorado that is focused on the discovery, development and commercialization of targeted small molecule drugs to treat patients afflicted with cancer. Array recently received approval and launched BRAFTOVI (encorafenib) and MEKTOVI (binimetinib) for the treatment of patients with BRAF mutated melanoma. These products have also been granted Breakthrough Therapy Designation by the FDA for BRAF mutated CRC.Summary:Residing in our Boulder, CO office, this role will provide project support for the Supply Chain and Manufacturing (SCM) team. Projects to be supported may include formulation development, technology transfer and scale up, process optimization, clinical manufacturing and supply, commercial manufacturing and supply, etc. Project scopes may include Drug Substance/API and Drug Product. Candidate will support the Supply Chain and Manufacturing (SCM) team.Responsibilities Creates, communicates, and follows up on action items and key deliverables through their closure/completion Executes assigned tasks to ensure project deliverables are met Disseminates project information internally as required Generates and tracks milestones; evaluates project issues and assists with their resolution Organizes and facilitates team meetings and presentations; generates meeting minutes and other project documents as required Ensures timely documentation and communication of decisions and updates on timelines and deliverables Coordinates and acts as a liaison between the project managers and SCM, Quality Assurance, Regulatory Affairs, Legal and external vendors Authors and/or implements documents, such as Change Controls, SOP's, Master Batch Records, etc. Track work orders and project spending Support shipment of compounds through preparation of supporting documentation, monitoring of shipments and shepherding through customs release Performs standard administration activities as requiredSkills and RequirementsRequirements: BS or equivalent preferably in Engineering, Chemistry, Biochemistry, or other related field 2 - 4 years related project management experience (preferably in pharmaceutical development) Ability to write clear, concise reports and business correspondence Expertise with Microsoft software (MS Word, Excel). Experience with Microsoft Project a plus. Ability to accept direction and guidance from more senior colleagues and managers Ability to support projects and meet established deadlines Ability to prioritize and implement multiple activities Strong attention to detail
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