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Sobi - Swedish Orphan Biovitrum AB (publ)

Associate Director – Project Management

Sobi - Swedish Orphan Biovitrum AB (publ)

Associate Director of Project Management at Sobi providing hands-on expertise for product launches. Leading project plans and cross-functional teams in the pharmaceutical industry.

Posted 5/27/2026full-timeRemote • Massachusetts • 🇺🇸 United StatesSenior💰 $150,000 - $190,000 per yearWebsite

About the role

Key responsibilities & impact
  • Provide hands-on project management expertise to ensure the successful, on-time launch of our commercial products, including but not limited to our uncontrolled gout asset (NASP)
  • Monitor progress, identify potential bottlenecks, and take proactive measures to ensure on-time completion of deliverables
  • Assist in the coordination of a diverse, cross-functional team including representatives from Marketing, Sales, Medical Affairs, Market Access, Commercial Insights and Analytics, Supply Chain and Regulatory Affairs
  • Construct and maintain comprehensive, cross-functional integrated project plans and timelines using project management software (SmartSheet)
  • Proactively identify, evaluate, and monitor project risks and issues, developing and implementing appropriate mitigation strategies and contingency plans to ensure seamless progress and goal attainment
  • Ensure effective, accurate, and timely communication of project status, challenges, and achievements to all stakeholders, including senior leadership, tailoring the message to the audience
  • Drive continuous improvement initiatives, implementing project management best practices and tools to enhance team efficiency and launch processes

Requirements

What you’ll need
  • Bachelor's degree required
  • Advanced degree (MS, MBA, PharmD, PhD) preferred
  • Minimum of 5 years of progressive experience in pharmaceutical or biotechnology project/program management
  • Consulting experience (with pharmaceutical launch engagements) a plus
  • Proven track record of successful contributions in the commercialization and launch of pharmaceutical products
  • Familiarity with regulatory submissions (e.g., NDA, BLA, MAA) and interactions with regulatory agencies is a plus
  • Expertise in project management methodologies, tools, and best practices
  • Strong facilitation presence with the ability to influence, motivate, and lead teams without direct authority
  • Exceptional organizational, time management, and problem-solving skills, with the ability to manage multiple priorities in a fast-paced environment
  • Outstanding verbal and written communication skills, capable of summarizing complex information clearly for diverse audiences
  • Proficiency in project management software (Smartsheet) and MS Office Suite

Benefits

Comp & perks
  • Competitive compensation for your work
  • Generous time off policy
  • Summer Fridays
  • Opportunity to broaden your horizons by attending popular conferences
  • Emphasis on work/life balance
  • Collaborative and team-oriented environment
  • Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
project managementregulatory submissionscommercializationpharmaceutical product launchrisk managementmitigation strategiesproject management methodologiesproblem-solvingtime managementfacilitation
Soft Skills
leadershipcommunicationorganizational skillsinfluencemotivationteam collaborationadaptabilitystakeholder managementcritical thinkingmultitasking
Certifications
Bachelor's degreeadvanced degree (MS, MBA, PharmD, PhD)