Senior Medical Science Liaisons (MSL) - Cardiovascular, Florida

About Mineralys Therapeutics

"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.

Mineralys is a fully remote company.

Our Medical Affairs team is hiring a Senior Medical Science Liaison in Florida!

This field-based medical expert will support the US Medical Affairs team and will focus on establishing, developing, and maintaining strong collaborative relationships through scientific engagement with Key Opinion Leaders and Healthcare Practitioners within the assigned territory. This field position requires a strong background in the pharmaceutical industry, understanding the complexities of healthcare systems, and requires experience in an MSL or MSL like role in cardiovascular disease.

• Build and maintain relationships with key opinion leaders (KOLs) and healthcare professionals within assigned region
• Primary point of contact for field medical and scientific inquiries
• Serve as subject matter expert at key medical and scientific conferences, advisory boards, roundtables, clinical investigator meetings, speaker training, and internal meetings
• Lead and/or participate in project teams that support MSL strategies and tactics as delegated by MSL leadership
• Identify and engage with healthcare stakeholders to educate and communicate clinical and scientific data, outcomes, and economic data to providers
• Deliver scientific presentations and training to diverse HCP audiences with the ability to summarize and communicate complex scientific information in an effective manner
• Serve as a strategic partner with internal cross-functional teams
• Support clinical trial site activities as needed and identify/ advocate for opportunities in investigator sponsored trial research
• Support continuing medical education (CME) requests and activities through unsolicited grants process
• Support field medical congress activities, and attend national, regional, and local meetings and medical congresses where appropriate to gather competitive intelligence, develop productive medical collaborations, and attend and report on educational sessions
• Gather, analyze, and communicate actionable insights from the field to inform company strategy, clinical challenges, and patient management trends
• Participate and contribute in cross-functional meetings, ensuring insights from the field are shared and discussed with Medical Affairs, R&D, Commercial, and other key internal stakeholders
• Ensure policies, procedures, and guidance are adhered to and Perform all Company business in accordance with all regulations (e.g. EEO FDA, OSHA, PDMA, EPA PhRMA, etc.)
• Contribute to medical affairs metrics, qualitative and quantitative MSL reports and SOPs for the MSL function. Document all field activities in accordance with company policies and regulatory requirements, ensuring compliance with industry standards