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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
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
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)