Asklepios BioPharmaceutical, Inc. (AskBio)

Associate Director, Program Management

Asklepios BioPharmaceutical, Inc. (AskBio)

full-time

Posted on:

Location Type: Remote

Location: Remote • 🇺🇸 United States

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Job Level

Senior

About the role

  • In partnership with the IPT Lead, define scope, objectives, and deliverables for product candidates in stages of clinical development
  • Create and maintain integrated development plans that accurately capture timelines, decision points (i.e., stage gates), resource needs, and budget for multiple clinical programs
  • Track and coordinate critical activities required to advance programs into early-stage and/or registrational clinical studies
  • Provide general operational support to the IPT, including risk identification/mitigation, problem-solving, communication, and contingency planning
  • In partnership with IPT lead, ensure the team is prepared for stage-gates and governance interactions, including content development, stakeholder management, and pre-reads
  • Deliver timely updates to key functional stakeholders, leadership, and governance boards covering program status, risks/mitigation, scope changes, etc.
  • Document IPT meeting minutes, key decisions, risks/issues, and action items
  • Ensure the team communicates effectively and collaboratively, implementing team building techniques where needed to establish and maintain a high-performing teams
  • Facilitate creation of program budgets, resource models and long-range plans
  • Define resource needs (FTEs and financial) for each stage of development
  • Ensure all critical program documentation is organized, accessible, and archived
  • In partnership with the PM Center of Excellence, develop, implement, and champion PM best practices, processes, and strategies within the IPT and supporting functions
  • Assist with implementation of stage-gates and IPT operating model, including education to the organizations through functional team sessions and meetings with stakeholders/teams

Requirements

  • Bachelor’s degree in a technical or life science discipline
  • 8+ years of experience within the pharmaceutical/biotechnology industry
  • 4+ years of project/program management experience
  • Excellent written and verbal communication skills with the ability to communicate effectively across disciplines and experience levels, including executive management
  • Experience in planning and/or managing cross-functional aspects of biopharmaceutical product development, including translational and clinical studies
  • Experience with SmartSheets and/or other project planning/management software
  • Ability to mentor, lead, and/or influence partners in a matrixed environment
  • Previous exposure to budgeting and resource management processes
Benefits
  • Equal Opportunity Employer
  • Reasonable accommodation for qualified individuals with disabilities

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
project managementprogram managementbudgetingresource managementclinical developmenttranslational studiesclinical studiesrisk identificationproblem-solvingstakeholder management
Soft skills
communicationteam buildingmentoringleadershipcollaborationorganizational skillsinfluencingcontingency planningdecision makingdocumentation
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