“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.
Our Medical Affairs team is growing, and we are currently seeking a MedComs Sr. Manager to join our diverse and dynamic team. In this role, you will be responsible for overseeing the development and dissemination of symposia, videos, podcasts and other medical education content to support our clinical research initiatives. Your expertise will be essential in ensuring that accurate, relevant, and up-to-date medical education is provided to internal stakeholders and external partners.
Principal Responsibilities
Deliver high-quality, impactful scientific content that support both internal stakeholders (e.g., Field Medical) and external stakeholders (e.g., healthcare professionals).
Assist with development, review and/or maintenance of product and disease-related slide kits, symposia, digital educatio
Leverage digital (SERMO, podcasts, videos), omnichannel tools, and AI-driven solutions to innovate and enhance Medical Communication strategies, ensuring impactful and data-driven engagement with healthcare professionals and stakeholders
Contribute to medical congress activities, as needed, including support for booth content, scientific content and session coverage; create post-congress summary materials
Own the development, pull-through and execution of the Scientific Narrative and Scientific Communication Platform (SCP).
Participate in the creation and execution of scientific content plan for the fiscal year, including alignment with the Medical Plan
Develop program specific scientific materials such as mechanism of disease or action graphics, data summary decks, and templates for company wide use.
Manage external vendors and agencies to deliver high-quality live and virtual medical education programs.
Monitor and assess the effectiveness of medical education initiatives and provide feedback to cross functional teams for continuous improvement.
Align with cross-functional teams to develop a dynamic and evolving Independent Medical Education program.
Skills and Attributes
Exceptional communication, negotiation, and stakeholder management skills.
Ability to lead/manage multiple projects and priorities in a fast-paced, matrixed environment
Champion unwavering commitment to scientific rigor and data-driven decision-making
Able to ascertain scientific accuracy, stakeholder relevance, and appropriateness of the various formats utilized across all the scientific content materials
Must have strong business acumen, ability to interface with matrix partners to make trade-off decisions by managing Medical Communications Asset/Indication-level budget and allocation of funds and resources to highest business priorities.
Able to manage budgets and vendors
Willingness to take on ad hoc work or special projects as needed.
Travel
This position requires up to 10 % travel. Frequently travel is outside the local area and overnight. Some of the travel may be international.
Education and Experience
Must have an advanced medical degree (MD, DO, or equivalent), PharmD or PhD.
3+ years of medical affairs experience in the Pharmaceutical/Biotechnology industry
Experience in hypertension, sleep apnea, chronic kidney disease, launch experience preferred
Experience in budget and vendor management
Proven success in a fast-paced, entrepreneurial, smaller company environment is highly desired.
Proven experience in working collaboratively and cross functionally across field medical teams, corporate affairs, clinical development, commercial, sales, market access and other key functions and demonstrated ability to inform and shape company/product strategy.
Demonstrated understanding of laws, regulations, standards, and guidance governing the conduct of publications.
Proven experience collaborating with cross-functional, international teams.
Strong understanding of compliance and regulatory frameworks governing scientific exchange.
Strong understanding of regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., GPP, ICH, PhRMA Code).
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: $165,000 - $180,000
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