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Job Overview
Location
Remote
Job Type
Full-time
Category
Other
Date Posted
January 5, 2026
Full Job Description
đź“‹ Description
- • Lead the strategic development and execution of all medical publications for Mineralys Therapeutics, ensuring that cutting-edge science on lorundrostat and the company’s aldosterone-targeted pipeline reaches global clinicians, researchers, and regulatory stakeholders in the clearest, most impactful way.
- • Own the end-to-end publication lifecycle—from gap analyses and publication plans through congress abstracts, peer-reviewed manuscripts, and digital enhancements—while aligning every deliverable with Medical Affairs objectives, corporate milestones, and emerging real-world evidence.
- • Serve as the primary interface between Medical Affairs, Clinical Development, Biostatistics, Regulatory, and Commercial teams, translating complex Phase II/III data on hypertension, CKD, and OSA into scientifically rigorous, compliant narratives that advance clinical practice and support market access.
- • Build and manage a high-performing internal publications team, plus external medical writing vendors and key opinion leader (KOL) steering committees, ensuring timelines, budgets, and quality standards exceed industry benchmarks and adhere to GPP3, ICMJE, and company SOPs.
- • Drive innovative dissemination strategies, including plain-language summaries, interactive visual abstracts, podcasts, and social-media-friendly infographics, to maximize reach among cardiologists, nephrologists, endocrinologists, and primary-care audiences worldwide.
- • Oversee congress planning and execution—identifying strategic symposia, late-breaker opportunities, and poster/oral sessions at ACC, ASN, ESH, ISH, and ADA—while coordinating embargo management and on-site medical communications support.
- • Establish and maintain a comprehensive publication tracker and KPI dashboard that provides real-time visibility into submission status, citation impact, and KOL engagement metrics, enabling data-driven decisions for future evidence-generation initiatives.
- • Champion publication ethics and transparency by ensuring all clinical trials are registered, results are posted on ClinicalTrials.gov and EudraCT, and authorship and contributorship disclosures meet or exceed industry standards.
- • Partner with HEOR and RWE teams to integrate health-economic and patient-reported outcome data into publications, demonstrating lorundrostat’s value proposition to payers, health-technology-assessment bodies, and global medical societies.
- • Mentor junior medical writers and associate directors, fostering a culture of scientific curiosity, continuous learning, and cross-functional collaboration that positions Mineralys as an employer of choice in the competitive biotech landscape.
- • Contribute to global launch-readiness efforts by aligning publication milestones with regulatory filing timelines, advisory-board feedback, and post-marketing study protocols, ensuring seamless transition from clinical development to commercial success.
- • Stay ahead of evolving FDA, EMA, and PMDA guidance on data disclosure, digital communications, and scientific exchange, proactively advising executive leadership on risk mitigation and opportunity capture.
- • Represent Mineralys at external advisory boards, steering committees, and scientific congresses, cultivating relationships with top-tier investigators, journal editors, and professional societies to amplify the company’s scientific voice and thought leadership.
- • Leverage advanced analytics (bibliometrics, altmetrics, social listening) to measure publication impact, refine messaging, and identify emerging scientific trends that inform future pipeline development and lifecycle management strategies.
🎯 Requirements
- • Advanced degree (PharmD, PhD, MD) in life sciences or medicine with 10+ years of biopharma medical publications experience, including 4+ years in a leadership role.
- • Demonstrated track record of strategic publication planning and execution across Phase II/III cardiovascular, renal, or metabolic programs.
- • Expert knowledge of GPP3, ICMJE, CONSORT, and global regulatory guidance on scientific disclosure and data transparency.
- • Proven ability to manage cross-functional teams, external agencies, and KOL networks within aggressive timelines and budgets.
- • Exceptional scientific writing, editing, and storytelling skills with meticulous attention to detail and compliance.
🏖️ Benefits
- • Fully remote-first culture with flexible scheduling and quarterly in-person team summits in Radnor, PA.
- • Competitive base salary, annual performance bonus, and equity participation in a high-growth clinical-stage company.
- • Comprehensive health, dental, vision, and mental-wellness coverage for employees and dependents from day one.
- • Annual professional-development stipend, paid attendance at major scientific congresses, and access to leading industry training platforms.
Skills & Technologies
Remote
About Mineralys Therapeutics, Inc.
Mineralys Therapeutics, Inc. is a biopharmaceutical company dedicated to developing targeted treatments for cardio-renal-metabolic diseases. Their scientific focus is on the critical role of aldosterone in these conditions, aiming to improve outcomes for individuals managing hypertension, chronic kidney disease (CKD), and related disorders. The company is advancing Lorundrostat, a therapeutic in its pipeline, to address dysregulated aldosterone as a driver of these serious health challenges. By leveraging evolving scientific insights, Mineralys Therapeutics is committed to bringing innovative solutions to patients, addressing unmet needs in cardiovascular and metabolic health.
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