Mineralys Therapeutics

Lead and optimize marketing review workflows, manage vendor relationships, and support the launch of a biopharmaceutical product. | 8+ years in pharma/biotech marketing operations, expertise in FDA promotional regulations, and experience with Veeva PromoMats. | “Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone. Its initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor. Mineralys is headquartered in Radnor, Pennsylvania. For more information, please visit https://mineralystx.com. Follow Mineralys on LinkedIn, Twitter and Bluesky” Mineralys is a fully remote company. As we prepare for our first commercial launch, we are seeking an experienced marketing operations leader who is energized by the opportunity to build from the ground up and help the organization establish foundational capabilities for launch and commercialization Reporting to the VP of Marketing, the Marketing Operations leader to play a critical role in enabling Mineralys Therapeutics’ first commercial launch. The Director, Marketing Capabilities and Operations will help build and lead the marketing operations framework required to support the successful launch of lorundrostat and establish scalable, compliant processes for commercialization. The Director will work cross‑functionally to introduce rigorous review governance, operational infrastructure, and workflows that maximize execution quality while supporting a fast‑moving, entrepreneurial launch environment. This is a high‑impact, high‑visibility role with a unique opportunity to shape the commercial foundation and trajectory of Mineralys’ first product launch. Key Responsibilities Serve as primary operational lead and chair for both PRC (promotional) and MRC (medical) workflows. Partner with the Head of Regulatory Ad Promo to design workflows, cadence, SOPs, and quality controls for both promotional and medical review. Coordinate reviewers, manage agendas, track decisions, and ensure timely, high quality reviews, and coordination of 2253 submissions. Align on reviewer expectations, timing, prioritization, and cross functional readiness Coordinate and support issue escalation and risk mitigation discussions for promotional and medical claims Oversee all routing, issue tracking, meeting facilitation, and documentation within Veeva PromoMats as well as system and software updates. Reviews submissions for accuracy and compliance with SOPs and facilitates/moderates reviews. Provides expert guidance and training to promotional material sponsors and agencies on submission of high-quality and compliant work, review cycle timelines, and planning for submission through review to approval. Marketing Production, Fulfillment & Deployment Oversee development-to-distribution workflows for all approved print and digital materials. Manage vendor relationships covering production, inventory, storage, ordering, and distribution. Lead quality assurance, version control, and compliance-driven lifecycle management. Work closely with marketing and field sales to ensure the field and customer-facing teams have timely, compliant materials. Governance, Process Optimization & Systems Ownership Build and maintain scalable SOPs, workflows, templates and governance frameworks. Enhance operational efficiency through continual evaluation and optimization of process, systems, and vendor models. Partner with Digital/Omnichannel, Sales Ops, and IT to ensure future integration across CRM, consent, data flows, and digital ecosystem. Budget & Vendor Leadership Own operations budget spanning PRC/MRC operations, production, and fulfillment. Own system configuration and administration for promotional material review and approval platforms Manage forecasting, tracking, and PO processes with discipline and transparency. Travel This position requires up to 10-20% travel. Frequently travel is outside the local area and overnight. Some of the travel may be international. Education and Experience 8+ years of pharma/biotech experience in marketing operations, medical/promotional review operations, or related commercial execution roles. Strong experience creating and leading PRC and MRC processes in regulated environments. Well versed in FDA promotional regulations with knowledge of submission requirements Expertise in Veeva PromoMats and related review/workflow tools. Experience supporting first commercial launches strongly preferred. Bachelor’s degree required. PM certification or experience preferred Builder mindset: Comfort navigating ambiguity, creating structure, and building scalable processes in a fast‑paced, high‑growth environment. Exceptional program and project management skills. Strong relationship‑builder and facilitator who can influence without authority. Detail‑driven, organized, and able to manage multiple complex workflows. Clear, concise communicator who thrives in a fast‑moving, high‑expectation environment. These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range: $200,000 - $220,000 #LI-REMOTE

Develop and execute promotional medical education strategies, build thought leader engagement programs, and support launch readiness in a pharmaceutical context. | Over 10 years of experience in pharmaceutical or biotech HCP marketing, with proven success in promotional medical education, thought leader engagement, and launch experience. | “Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone. Its initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor. Mineralys is headquartered in Radnor, Pennsylvania. For more information, please visit https://mineralystx.com. Follow Mineralys on LinkedIn, Twitter and Bluesky” Mineralys is a fully remote company. As we prepare for our first commercial launch, we are seeking an experienced marketing leader who is energized by the opportunity to build from the ground up, establish foundational capabilities, and shape the promotional medical education strategy for a best‑in‑class launch. Reporting to the VP of Marketing, the Director, HCP Marketing & Thought Leader Engagement will serve as the strategic and operational leader responsible for defining and executing Mineralys’ promotional medical education and thought leader strategy across medical congresses, KOL engagement, advisory boards, speaker programs, and promotional medical education. This person will serve as the commercial lead for LCM planning and work cross-functionally to provide strategic insight into unmet needs, real world gaps, and future areas of opportunity. This role plays a critical launch role establishing Mineralys within the cardio renal metabolic (CRM) and hypertension communities. We are seeking a leader with deep pharmaceutical marketing expertise, ideally with chronic care and launch experience, to ensure all engagement activities support pre-launch efforts, inform brand strategy, and accelerate launch readiness. The ideal candidate can operate strategically while executing with precision in a lean, fast‑moving, launch‑focused environment. Key Responsibilities Developed and launched a comprehensive Promotional Medical Education platform encompassing a Congress Strategy, Speakers Bureau, National Broadcasts, and Third-Party Educational Content for both pre-launch unbranded and branded initiatives Lead strategy, design, and execution of national and regional advisory boards, aligning to evidence gaps and shaping scientific narrative. Develop a structured KOL engagement roadmap across pre‑ and post‑approval phases and foster relationships with national and regional thought leaders in hypertension and CVRM care Build Mineralys’ first speaker bureau including recruitment, evaluation, training, content development, and performance monitoring Develop and execute industry leading non-personal promotional medical educational programs Lead commercial efforts to provide strategic insight into unmet needs, real‑world gaps, and future opportunity areas into clinical development and investment decisions to ensure commercially competitive clinical profiles for LCM planning Work cross‑functionally to pressure‑test potential LCM scenarios and support evidence‑generation prioritization. Collaborate cross-functionally to build processes and ensure compliance in HCP contracting, fair‑market‑value adherence, Sunshine Act reporting, promotional content review, and program execution Travel This position requires up to 30-40 % travel. Frequently travel is outside the local area and overnight. Some of the travel may be international. Education and Experience 10+ years of experience in pharmaceutical or biotech HCP marketing, professional education, promotional medical communications, or thought‑leader engagement. Significant experience in building promotional medical education and execution including congress strategy and thought leader engagement. Demonstrated expertise in speaker bureau strategy and management, including peer‑to‑peer program design and execution. Proven ability to build new capabilities and operating models in a launch or high‑growth environment. Demonstrated experience partnering with national and regional thought leaders to inform brand strategy and launch execution in chronic care disease areas. Experience in cardiovascular, nephrology, metabolic disease, or hypertension preferred. Previous launch experience preferred. Comfort navigating ambiguity, creating structure, and building scalable processes in a fast‑paced, high‑growth environment. Strong strategic thinking, cross‑functional leadership, and executive presence. Bachelor’s degree required; MBA or advanced degree preferred. These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range: $200,000 - $220,000 #LI-REMOTE

Build and execute digital and omnichannel strategies, oversee digital ecosystem, and lead digital media planning and customer journey orchestration. | Requires 8-10+ years in digital marketing, experience in pharma/biotech, leading product launches, and proficiency with regulated industry marketing platforms. | “Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone. Its initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor. Mineralys is headquartered in Radnor, Pennsylvania. For more information, please visit https://mineralystx.com. Follow Mineralys on LinkedIn, Twitter and Bluesky” Mineralys is a fully remote company. As we prepare for our first commercial launch, we are seeking an experienced digital leader who is energized by the opportunity to build from the ground up, establish foundational capabilities, and shape the digital ecosystem for a best‑in‑class launch. Reporting to the Head of Consumer and Patient Marketing, the Omnichannel & Digital Marketing lead will architect the HCP & Patient digital strategy, stand up new platforms and processes, lead media and content planning, and drive the integration of digital channels into the broader commercial launch plan. This role requires a hands-on builder with deep expertise in digital marketing, omnichannel orchestration, media activation, analytics, and innovation. You'll operate strategically while executing with precision in a lean, fast-moving, launch-focused environment. If you thrive on creating something new and owning the outcome, this is your opportunity. Principal Responsibilities Build the Digital & Omnichannel Foundation Develop and execute digital and omnichannel strategy aligned with customer needs, brand objectives, and launch goals. Evaluate, select, and operationalize CRM, marketing automation, analytics platforms, content management systems (CMS), digital asset management (DAM), consent management, and reporting tools in partnership with IT and agency partners. Oversee owned, earned, and paid digital ecosystem (websites, CRM, email, paid media, SEO/SEM, social, programmatic) to ensure channel integration and continuous performance optimization. Establish digital standards, operating models and processes that scale with the organization. Monitor emerging digital trends and technologies to identify opportunities for enhanced customer engagement through AI, digital health tools, telehealth integrations, and new channels. Establish UX/UI standards across all digital properties, ensuring intuitive navigation, accessibility compliance, and consistent brand experience. Media, Content & Engagement Strategy Lead digital media planning and optimization, collaborating with agency partners to refine audience strategies, channel mix, and activation plans. Build audience targeting, segmentation, and personalization strategies leveraging 1P (first‑party) and 3P (third‑party) data through healthcare data partnerships and privacy-safe activation methods. Design personalized, insight-driven content strategies and modular assets to support omnichannel engagement across HCP and patient journeys in collaboration with HCP and Consumer Brand Leads. Own digital and omnichannel budgets, including scenario planning, investment allocation, forecasting, and ROI measurement. Customer Journey & Omnichannel Orchestration Map end‑to‑end HCP and patient journeys, identifying key moments, triggers, and channel opportunities. Design digital–field orchestration including CLM content, rep‑triggered email, automated nurture sequences, behavioral triggers, next‑best‑action logic, field alerts, and closed‑loop reporting—ensuring seamless data flows between CRM, marketing automation, web, and analytics. Integrate digital touchpoints with field activities, patient support services, and brand objectives to deliver a seamless, personalized experience. Develop digital tools, training, and processes to enable Field Sales and MSLs as integrated touchpoints in the customer journey. Partner with IT, Analytics, and agency partners to ensure strong technical integration and visibility across the customer journey. Insights, Analytics & Measurement Drive development of KPIs, dashboards and measurement frameworks; define leading/lagging indicators for launch. Lead a robust test‑and‑learn agenda to continuously optimize channel performance and budget allocation. Translate data into actionable insights and next‑step recommendations that inform brand strategy and commercial planning. Cross-Functional Leadership & Vendor management Build and oversee the vendor/agency ecosystem required for launch success; define scopes, operating cadences, and quality benchmarks. Embed digital best practices and a culture of omnichannel thinking across the commercial organization. Serve as a strategic partner to the field teams, ensuring omnichannel insights and digital resources support field effectiveness. Compliance & Governance Ensure all digital programs and content adhere to FDA guidelines, privacy laws (e.g., HIPAA), data governance principles, and internal policies. Lead consent management and privacy-compliant data strategies that future-proof targeting capabilities amid evolving privacy regulations. Travel This position requires up to 20-30 % travel. Frequently travel is outside the local area and overnight. Some of the travel may be international. Education and Experience Required: Bachelor's degree required, MBA or advanced degree in Marketing, Digital Marketing, or related field preferre 8 - 10+ years of progressive experience in digital marketing, with at least 5 years in pharmaceutical/biotech industry Proven experience leading commercial product launches in a digital capacity Deep expertise in omnichannel marketing platforms (e.g., Veeva CRM, Salesforce Marketing Cloud, Adobe Experience Cloud) Strong understanding of HCP and patient marketing in regulated industries Experience with marketing analytics, attribution modeling, and ROI measurement Track record of building digital capabilities from the ground up in lean organizations Deep understanding of pharmaceutical commercial models, FDA promotional requirements, privacy laws (e.g., HIPAA), and digital governance Preferred: Experience with AI-powered personalization, predictive analytics, generative AI applications Track record of implementing consent management platforms and navigating cookie deprecation/privacy-first marketing strategies Experience with patient advocacy partnerships, HCP influencer programs, and amplification strategies These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range: $200,000 - $220,000 #LI-REMOTE

Lead global CMC regulatory strategy and manage regulatory submissions for biopharmaceutical products. | Extensive experience in pharmaceutical/biotech CMC regulatory leadership, with proven agency interaction skills and knowledge of global regulatory requirements. | “Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone. Its initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor. Mineralys is headquartered in Radnor, Pennsylvania. For more information, please visit https://mineralystx.com. Follow Mineralys on LinkedIn, Twitter and Bluesky” Mineralys is a fully remote company. The Senior Director, CMC (Chemistry, Manufacturing, and Controls) Regulatory is responsible for leading the development, execution, and maintenance of global CMC regulatory strategy to support clinical development, registration, commercialization and lifecycle management of Mineralys products. This role provides strategic and operational leadership for all CMC-related regulatory activities, supporting cross-functional decision-making by providing regulatory guidance, ensuring compliance of CMC documentation and high-quality submissions that meet global regulatory requirements and support business objectives. The Sr. Director partners closely with CMC, Quality, and external partners to ensure alignment of CMC documentation, regulatory strategy, product lifecycle planning and management. Key Responsibilities Strategic Leadership Develop and implement global CMC regulatory strategies aligned with clinical development, manufacturing, commercialization, and other business objectives. Provide regulatory intelligence on global CMC requirements and emerging regulatory trends. Represent the company in regulatory agency interactions and strategic meetings on CMC related topics. Regulatory Submissions & Lifecycle Management Oversee preparation, review, and approval of CMC components in regulatory submissions (IND/CTA, NDA/MAA, post-approval lifecycle management). Advise all CMC related functions (Process Development, Analytical Development, Quality Control) on the preparation of IND/CTA and NDA/MAA dossiers to ensure timely delivery of quality documents for submission. Liaise with global regulatory authorities as needed for all CMC aspects pertaining to drug development including resolution of key regulatory issues. Lead CMC responses to regulatory agency inquiries and deficiency letters. Cross-Functional Collaboration Serve as CMC RA subject matter expert in cross-functional project teams (R&D, Quality, Manufacturing, Supply Chain). Provide counsel, training, and interpretation of FDA and other regulatory guidance to company personnel. Build partnerships and foster collaboration with key stakeholders to ensure business goals are met. Guide integration of CMC regulatory considerations early in development and manufacturing decisions. Provide regulatory impact assessments and guidance for manufacturing changes, technology transfers, and lifecycle initiatives. Provide CMC review/input for clinical study protocols, investigator brochures, and other relevant reports. Process & Best Practices Establish and maintain CMC RA procedures and best practices to support submission readiness and compliance. Develop processes, systems, and infrastructure to assure CMC regulatory compliance. Monitor new regulations, guidance and interpret impact on company programs. Qualifications Education Advanced degree (MS, PhD, PharmD) in Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or related scientific discipline; Bachelor’s degree with extensive experience acceptable. Experience Minimum 10 + years of pharmaceutical/biotech experience with 8 + years CMC regulatory experience. Proven record of leading global CMC strategy, submission, and agency interactions (FDA, EMA, PMDA etc.) in both pre- and post-marketing settings. Strong knowledge of global CMC regulatory requirements, ICH guidelines, and submission standards. Demonstrated ability to interpret and apply regulatory guidance to complex CMC issues and lifecycle activities. Experience with regulatory submission management tools and electronic submission systems. Solid understanding of quality management systems including change controls, documentation management systems. Ability to work effectively in a fast-paced and results-focused environment and on matrix teams. Core Competencies Strategic Planning Regulatory Risk Assessment & Management Project & Time Management Stakeholder Engagement Cross-Functional Collaboration & Influence Excellent Communication Skills Travel This position requires up to 20% travel. Frequently travel is outside the local area and overnight. These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range: $240,000 - $270,000 #LI-Remote

Lead regulatory activities for promotional and medical materials, ensuring compliance with FDA and industry standards, and collaborate cross-functionally to support product launch. | 8+ years in regulatory, with 5+ years in Ad & Promo within biopharma, deep FDA regulation knowledge, and launch experience. | “Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone. Its initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor. Mineralys is headquartered in Radnor, Pennsylvania. For more information, please visit https://mineralystx.com. Follow Mineralys on LinkedIn, Twitter and Bluesky” Mineralys is a fully remote company. The Senior Director, Advertising & Promotion, Regulatory Affairs (Ad & Promo) will lead all regulatory activities related to medical and promotional material development, review, and external communications for Mineralys as it advances toward commercialization. This individual will serve as the primary regulatory representative on the Medical, Legal and Regulatory (MLR) team, ensuring that all promotional, non-promotional and scientific exchange materials adhere to internal policies, relevant laws, FDA regulations, and industry standards. This is a highly visible, hands-on role ideal for a strategic, detail-oriented, and collaborative regulatory leader who thrives in a fast-moving, small-company environment and is comfortable building Ad & Promo infrastructure under launch timelines. Key Responsibilities Strategic Leadership Serve as the Regulatory lead on the MLR team, providing timely, compliant strategic guidance for all promotional and non-promotional materials development. Interpret and apply FDA Advertising & Promotion regulations, guidance, OPDP expectations and enforcement trends, to company materials. Serve as a strategic thought partner with Marketing and Medical Affairs to develop compliant and compelling promotional and medical strategy and framework ahead of launch. MLR Review and OPDP Interactions Collaborate cross-functionally with Medical Affairs, Commercial, Legal, Clinical Development, and agency partners on messaging and claims substantiation. Provide regulatory guidance on digital and omnichannel content, including modular content, rapid update scenarios, and social media platforms Review all relevant materials, including but not limited to digital and print assets, HCP and patient-facing materials, disease awareness, sales training, company-controlled medical education, press releases, social media, and investor communications (as appropriate) to ensure compliance. Partner with Marketing Operations to ensure seamless MLR execution, workflow design, SOPs, timelines, and cross-functional coordination. Lead interactions with OPDP, including advisory comments, submissions, and correspondence. Orchestrate promotional audits and monitoring, and corrective actions as appropriate. Monitor and interpret regulatory developments related to Advertising & Promotion and proactively update the organization regarding implications. Support internal training on Advertising & Promotion requirements. Cross-Functional Leadership Build strong relationships across Medical, Legal, Commercial, Clinical, and Compliance functions, providing balanced solutions-oriented guidance. Facilitate discussions around regulatory risk tolerance and best practices to enable compliant and competitive brand execution. Qualifications Education & Experience Bachelor’s degree required; advanced scientific degree (PharmD, PhD, JD, or MS) preferred. 8+ years regulatory experience, including 5+ years in Ad & Promo within the biopharmaceutical industry. Direct experience leading U.S. regulatory review of promotional materials and interfacing with OPDP; global experience a plus. Launch and pre-launch experience is strongly preferred. Skills & Competencies Deep knowledge of FDA regulations (21 CFR Parts 201, 202, and applicable postmarketing submission requirements), promotional guidance including CFL, and enforcement trends. Strong scientific understanding of clinical data with the ability to interpret, analyze, and translate complex findings into compliant messaging. Demonstrated ability to collaborate cross-functionally and influence stakeholders without direct authority. Exceptional communication skills; able to deliver clear, concise, and actionable guidance. Comfort working in a small, fast-paced, matrixed biotech environment. Ability to balance scientific accuracy, commercial objectives, and regulatory risk. Experience supporting DTC and HCP campaigns. Ability to work independently with minimal oversight. Travel This position has approximately 10% travel. Frequently travel is outside the local area and overnight. These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range: $275,000 - $290,000 #LI-Remote

Lead the development of healthcare professional brand strategy and activation, ensuring cross-functional alignment for launch planning. Oversee the creation and execution of promotional assets and evaluate the effectiveness of strategies through campaign measurement. | Candidates should have an MBA or bachelor's degree with 8+ years of experience in the pharmaceutical or biotech industry, including at least 5 years in marketing strategies. Previous launch experience and cardiovascular expertise are highly preferred. | Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit https://mineralystx.com. Follow Mineralys on LinkedIn. Reporting to the VP of Marketing, the Director/ Sr. Director, HCP Marketing will lead healthcare professional brand strategy and develop go-to-market launch initiatives to achieve launch success. The ideal candidate will be a self-starter with deep experience in HCP marketing, including launch planning, messaging and creative development, and cross-functional leadership. Previous launch leadership and cardiovascular experience is strongly preferred. This role is perfect for someone who thrives in an entrepreneurial setting and is excited to shape a brand from day one. Principal Responsibilities Lead the development of HCP brand strategy and activation, including positioning, messaging, and tactical plans. Oversee creation and execution of a compelling creative campaign and HCP promotional assets. Partner on HCP focused market research efforts to ensure decisions are well-informed and driven by customer insights to accelerate brand growth and engagement. Serve as the brand lead and primary point person for launch planning, ensuring cross-functional alignment and aligned launch metrics. Work closely with internal teams (Medical, Legal, Regulatory, Compliance) to ensure compliant and aligned messaging Manage relationships with external vendors and agency partners Partner with Sales, Sales Training, and Commercial Operations to develop and optimize field force initiatives to support brand messaging and engagement. Evaluate the effectiveness of promotional strategies through campaign measurement and metrics development to ensure positive return on investment and achievement of brand objectives. Skills and Attributes Flexibility to adapt to a fast-changing, ambiguous environment in an organization without fully established procedures Velocity – Drive Speed with Purpose Foresight & Acceleration Execution Under Tight Timelines Clear Decision-Making in Ambiguity Data-Driven Decision Making – Ground Strategy in Evidence Subject Matter Intelligence & Precedent-Based Reasoning Data Interpretation Metrics-Oriented Agile Mindset – Embrace Iteration and Change Adaptability to Shifting Development Plans Iterative Planning & Engagement Frictionless Execution – Simplify the Path to Results Operational Clarity & Precision Lean, Cross-Functional Collaboration Strategic Communication Autonomy – Lead with Ownership and Accountability Self-Directed and Proactive Trusted Decision Maker Leads from the Front Execution that Delivers Value Define success up front Follow through with discipline Deliver results that move the business Travel This position requires up to 20 % travel. Frequently travel is outside the local area and overnight. Some of the travel may be international. Education and Experience MBA or bachelor’s degree plus 8+ years of pharmaceutical or biotech industry experience with at least 5 years building and executing marketing strategies Launch experience and commercialization of new products preferred Cardiovascular experience is highly preferred. Demonstrated ability to develop and execute brand strategy and promotional campaigns in a fast-paced environment. Strong project management skills, with the ability to manage multiple priorities and stakeholders. Experience leading cross-functional teams and agency partners. A self-starter mindset with high personal accountability, resourcefulness, and a collaborative spirit. Excellent communication and presentation skills. These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range: $175,000 - $250,000 #LI-Remote