Senior Medical Science Liaisons (MSL) - Cardiovascular, Arizona

Mineralys Therapeutics

8d•$190,000 - $225,000•Remote

About The Position

Mineralys Therapeutics is a clinical-stage biopharmaceutical company developing medicines targeting hypertension and related comorbidities, including chronic kidney disease, obstructive sleep apnea, and other diseases driven by dysregulated aldosterone. Its initial product candidate is lorundrostat, a proprietary, orally administered, highly selective aldosterone synthase inhibitor. Mineralys is headquartered in Radnor, Pennsylvania, and is a fully remote company. The Senior Medical Science Liaison is a field-based medical expert supporting the US Medical Affairs team in Arizona. The role establishes, develops, and maintains collaborative relationships with Key Opinion Leaders and healthcare practitioners through scientific engagement within the assigned territory. It requires a strong pharmaceutical-industry background, an understanding of healthcare-system complexities, and experience in an MSL or MSL-like role in cardiovascular disease. The position involves approximately 50–70% travel.

Requirements

Pharm.D., Ph.D., M.D., or D.O.; other doctoral degrees may be considered.
At least 5 years of current MSL experience for the Senior MSL level.
Experience in an MSL or MSL-like role in cardiovascular disease.
Experience with all phases of Key Opinion Leader development and healthcare practitioner engagement, including drug launches.
Strong ability to drive cross-functional collaboration, deliver high-quality scientific insights, and achieve measurable outcomes aligned with corporate goals.
Strong interpersonal skills, including excellent verbal and written communication and peer-to-peer professional collaboration.
Located within driving distance of a major international airport.
Valid US driver's license and ability to travel without restrictions.
Willingness to travel approximately 50–70%.

Nice To Haves

Cardiology, renal, or metabolic experience.
At least 5 years focused on clinical practice, clinical research, or medical research.
Post-doctoral training, including residencies or fellowships, as medically related experience.

Responsibilities

Build and maintain relationships with Key Opinion Leaders and healthcare professionals within the assigned region.
Serve as the primary point of contact for field medical and scientific inquiries.
Serve as a subject matter expert at medical and scientific conferences, advisory boards, roundtables, clinical investigator meetings, speaker training, and internal meetings.
Lead or participate in project teams supporting MSL strategies and tactics, as delegated by MSL leadership.
Identify and engage healthcare stakeholders to communicate clinical, scientific, outcomes, and economic data to providers.
Deliver scientific presentations and training to diverse healthcare practitioner audiences, effectively summarizing complex scientific information.
Serve as a strategic partner to internal cross-functional teams.
Support clinical trial site activities as needed and identify and advocate for investigator-sponsored trial research opportunities.
Support continuing medical education requests and activities through the unsolicited grants process.
Support field medical congress activities and attend national, regional, and local meetings and medical congresses as appropriate to gather competitive intelligence, develop medical collaborations, and report on educational sessions.
Gather, analyze, and communicate actionable field insights to inform company strategy, clinical challenges, and patient-management trends.
Participate in cross-functional meetings and share field insights with Medical Affairs, R&D, Commercial, and other internal stakeholders.
Adhere to company policies, procedures, guidance, and applicable regulations, including EEO, FDA, OSHA, PDMA, EPA, and PhRMA requirements.
Contribute to Medical Affairs metrics, qualitative and quantitative MSL reports, and MSL-function SOPs.
Document field activities in accordance with company policies and regulatory requirements and ensure compliance with industry standards.