About The Position

At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients. Our mission and culture at Sobi North America get us excited to come to work every day, but here are a few more reasons to join our team: Competitive compensation for your work, Generous time off policy, 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. Sobi is seeking a passionate, strategic marketer for the Director/Senior Director, US Marketing role. This highly visible position will represent the first US marketing hire supporting the potential launch of a novel, oral therapy for a severe, rare form of gout. You will play a critical role in developing and executing the pre-launch and launch strategies for this asset across HCP and patient/consumer audiences. You will lead cross-functional teams, leveraging previous experience in disease-state strategy, customer segmentation, omnichannel, and branded promotion. The ideal candidate will have a proven track record of successfully launching and promoting therapies in the US rheumatology space. This role will report to the Executive Director, Immunology/Rheumatology Marketing. It will start as an individual contributor role with the potential to grow into a role with direct reports. This role is remote with a preference for candidates in/around Waltham, MA, to come into the office several times a month.

Requirements

  • Bachelor’s degree in Marketing, Business, or Life Sciences
  • 15+ years of relevant pharmaceutical or biotech industry experience
  • 5+ years of progressive people management experience in marketing roles of increasing responsibility
  • Broad commercial experience across U.S. HCP marketing, patient marketing, and omnichannel marketing required
  • Proven success leading U.S. product launches from pre‑launch through commercialization, managing high‑impact projects and tactics
  • Demonstrated ability to manage complex projects through Legal, Medical, and Regulatory review and approval
  • Strong understanding of key laws and regulations impacting the pharmaceutical industry (PhRMA Code, HIPAA, FD&C Act, Anti‑Kickback Statute) with a commitment to ethical and compliant practices
  • Experience working in a small‑to‑mid‑sized biopharmaceutical company is required
  • Ability to travel up to 30%
  • Strategic thinker with the ability to translate insights into actionable marketing plans and tactics
  • Comfortable translating complex clinical information, such as mechanism of action, trial designs, and efficacy/safety data, for both HCP and consumer audiences
  • Must thrive in a fast‑paced, results‑driven environment, with the ability to manage ambiguity
  • Proactive self-starter who thrives both independently and in team settings; skilled at leading without formal authority
  • Adept at shifting between strategic leadership and hands-on execution as needed
  • Experienced in managing teams and influencing stakeholders across matrixed organizations
  • Strong project, vendor, and agency management skills, including resource allocation and budget oversight
  • Excellent communicator with proven ability to influence across functions and all organizational levels

Nice To Haves

  • MBA or other advanced degree preferred

Responsibilities

  • Develop initial launch strategy and high-level launch plan
  • Refine commercial opportunity assessment, including potential use cases across the disease continuum/lines of therapy
  • Lead development of initial product value proposition, including positioning/copositioning strategy and asset-specific lexicon recommendations
  • Develop initial recommendations related to HCP and patient prioritization and go-to-market model requirements
  • Lead cross-functional working group to align on a product SWOT and strategic imperatives, identifying major investment requirements e.g., DTC, media, field sales, patient services
  • Codify and maintain key launch strategies and assumptions in a brand plan
  • Build and work with cross-functional partners to execute a market development strategy inclusive of disease state education, PR/media, Ad Boards, and KOL/professional society engagement
  • Serve as the US commercial representative on the labeling strategy workstream
  • Collect stakeholder insights, monitor the competitive environment, and commission market research to inform the projects above
  • Lead the process to select key agency partners who will support the launch
  • Partner and align with cross-functional and global partners to establish launch readiness milestones, requirements, and timelines
  • Collaborate closely with the global team on the development of early US promotional assets e.g., brand book, logo, etc.
  • Develop and manage OPEX forecasts
  • Cultivate strong relationships and drive collaboration with all cross-functional partners, including sales, global commercial, regulatory, legal and compliance, medical, commercial operations, patient advocacy, patient services, field reimbursement, medical affairs, and market access
  • Lead branded marketing efforts for the asset post-PDUFA, inclusive of brand plan, promotional campaign, and materials development, and omni-channel strategies
  • Collaborate with field teams to identify best practices, uncover needs/trends, and build relationships to improve consistency of brand strategy execution
  • Partner with analytics and market research to distill insights, validate business opportunities, optimize marketing mix, and monitor return on investment (ROI) of marketing programs
  • Think holistically about the business and closely monitor performance against key metrics, taking accountability for driving the success of initiatives over the long-term in a competitive market
  • Lead all national congress participation, including contracting, booth design, and internal coordination

Benefits

  • Competitive compensation for your work
  • Generous time off policy
  • 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
  • A comprehensive and industry-competitive total rewards package
  • A competitive 401(k) match to support your financial future
  • Tuition and wellness reimbursements to invest in your personal and professional growth
  • A comprehensive medical, dental, and vision package to prioritize your health and well-being
  • Additional recognition awards to celebrate your achievements
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