via Adp
$85K - 130K a year
Lead US brand plan implementation and launch campaigns for MOLBREEVI with cross-functional collaboration and regulatory compliance.
Bachelor's degree and 5+ years pharma/biotech marketing experience with proven commercial product launch skills.
Reporting to the Executive Director, Global Marketing, the Senior Product Manager, US Commercial plays a key role in tactical implementation of the potential launch of MOLBREEVI*TM (molgramostim inhalation solution), an investigational therapy for treating autoimmune pulmonary alveolar proteinosis (aPAP). This role is critical in guiding the development and implementation of the US Brand Plan to ensure a successful market introduction. The position focuses on executing innovative and impactful initiatives for healthcare professionals (HCPs) and patients, managing the marketing mix, and collaborating cross-functionally with various departments to meet brand and company objectives. Responsibilities * Under the guidance of the Executive Director, Global Marketing, assist in developing the strategic US brand plan for MOLBREEVI, including market opportunity identification, market-shaping, positioning, messaging, campaign development, and segmentation * Optimize Disease State Awareness campaigns to increase market impact * Collaborate with opinion leaders and cross-functional teams to develop and gain approval for core promotional programs and tactics, ensuring launch readiness * Lead commercial execution at key conferences, society meetings, and educational initiatives * Contribute to the design and development of exceptional patient services and specialty pharmacy programs * Create and implement marketing and sales training materials * Develop and execute print, digital, and social media tactics for both HCPs and patients * Serve as a brand expert with deep knowledge of disease state, treatment landscape, patient journey, and market trends * Oversee partners to ensure strategic alignment and timely, budget-compliant execution of programs and tactics * Ensure all Medical Legal Regulatory (MLR) review processes are followed, and all programs are compliant with legal guidance and corporate policies * Serve as the primary coordinator for Medical, Legal, and Regulatory (MLR) review, managing workflows and timelines while partnering with cross-functional teams to ensure all materials and programs meet legal, regulatory, and corporate compliance standards. * Manage funds and resources efficiently and with an entrepreneurial approach * Other duties and projects as assigned. Required Qualifications * Bachelor’s degree required * 5+ years pharma/biotech industry experience required * HCP and/or patient marketing experience required * Commercial launch experience required; rare disease commercial launch experience strongly preferred * Demonstrated experience in driving performance and fostering collaboration * Ability to embrace teamwork and project management within a collaborative environment * Demonstrated analytical skills with regards to market research and key business insights * Strong interpersonal and communication skills and the ability to effectively drive performance * Excellent written and verbal communication skills in English * Ability to move nimbly between strategic thinking and tactical details to execute with excellence * Ability to thrive in a fast-paced, entrepreneurial environment. * Experience in managing external partners (e.g., consultants, vendors, agencies, etc.) * Proven ability to develop exceptional relationships and have an impact on others * Experience working in a start-up and/or mid-cap sized company highly desired Location and Travel * This role is remote within the US and requires availability to work US Eastern Time Zone. * Occasional travel may be required to the Yardley office, conferences, or other events, up to 25% of the time. Savara provides comprehensive benefits including: * Highly competitive medical, dental, and vision coverage * Flexible Spending Accounts for health care and dependent care expenses * Paid time off and paid holidays, including Dec 24-Jan 1 * Paid parental leave * 401k with highly competitive match * Life, AD&D, STD and LTD insurance coverage Savara’s compensation can include an hourly rate, bonus, and equity. The salary range for this role is $135,000 to $155,000. About Savara: Savara is a clinical-stage biopharmaceutical company focused on rare respiratory diseases. Our lead product candidate, MOLBREEVI*, is an inhaled recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF) in Phase 3 development for autoimmune pulmonary alveolar proteinosis (autoimmune PAP). MOLBREEVI* is delivered via a proprietary investigational eFLOW® Nebulizer System (PARI Pharma GmbH) specifically developed for inhalation of MOLBREEVI*. Our management team has significant experience in orphan drug development and pulmonary medicine, identifying unmet needs, and effectively advancing product candidates to approval and commercialization. Our goal is to become a leader in rare respiratory disease therapeutics through the development and commercialization of novel, best-in-class medicines that address unmet medical needs in this field. Savara is an equal opportunity employer. *MOLBREEVI is the proposed trade name for molgramostim inhalation solution. It is not approved in any indication. MOLBREEVI is a trademark of Savara Inc. #LI-Remote
This job posting was last updated on 8/26/2026