• The Senior Scientific Director is responsible for the planning, development, and oversight of scientific content for an assigned account or accounts across various therapeutic areas. • Leading assigned accounts, leading client interactions and brand strategy. • Leading the scientific portion of brand planning and business development. • Managing resource allocation, partnering with client services to develop SOWs and timelines, and identifying areas for new and organic growth.

Senior Medical Science Liaisons(MSL) - Cardiovascular, Detroit Region US Remote “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 hiring Senior Medical Science Liaison's across the US! Focusing on the Detroit, Michigan region. These field-based medical experts 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 Requirements: - Pharm.D., Ph.D., M.D. or D.O. (other doctoral degrees considered) - For a Senior MSL level we require 5+ years of current MSL experience, and 3 to 5 years of current MSL experience for a Medical Science Liaison in Scientific/Medical Affairs at a biotech or pharmaceutical company - Cardiology/Renal/Metabolic experience preferred. - 5+ years focused on clinical practice, clinical research, or medical research a plus - Experience in a medically related field can include post-doctoral training (i.e., residences and/or fellowships) - Experience with all phases of KOL development and HCP engagement with experience with drug launches - Skilled in driving cross-functional collaboration, delivering high-quality scientific insights, and consistently achieving measurable outcomes aligned with corporate goals. - Strong interpersonal skills including excellent verbal and written communication and peer-to-peer professional collaborations Must be located within driving distance of a major international airport; approx. 50 - 70% travel. Valid US driver’s license required, ability to travel without restrictions. 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: $190,000 - $225,000 #LI-Remote

• Lead the full lifecycle development of healthcare nutrition products, including thickened liquids, texture-modified foods, oral nutritional supplements, and hydration solutions for dysphagia patients. • Ensure all products meet clinical requirements for safety, efficacy, palatability, and compliance with IDDSI standards. • Drive formulation strategies that balance nutritional adequacy, sensory acceptance, stability, and ease of use in clinical and homecare settings. • Collaborate with Operations and Quality to ensure scalable, compliant manufacturing processes. • Build a robust innovation pipeline addressing unmet needs in dysphagia, malnutrition, and related conditions.

• Identify operational needs for upcoming projects, track and review current assignments for CAT Operations staff • Resource CAT study projects as Resource Manager • Engage as Subject Matter Expert (SME) for CAT Operations activities • Provide operational oversight for designated CAT study projects • Engage in and coordinate resourcing activities for all CAT awarded projects • Identify training and skills gaps among staff; coordinate and assist with learning opportunities to enhance operations staff knowledge and skills of industry related regulations, processes, materials, and guidelines • Actively identify and engage in process improvement activities • Participate in QMD reviews and new QMD development • Author, collaborate, and review QMD documents and guidance documents • Coordinate and manage CAT Operations team meetings • Active engagement and oversight of study risk assessments, as they relate to operational activities • Work with department leaders to ensure alignment among CAT operational and clinical services • Lead and/or contribute to departmental initiatives that aim to implement policies, methods, techniques to contribute to existing service areas and department growth • Accountable for oversight of CAT study deliverables from Launch process to study close out • Assist and collaborate with Operations staff, Project Management, Contracts on vendor and study budget development, scope of work revisions, tracking and compliance • Assist in vendor management related concerns, including involvement with escalations, Vendor Management and Quality Assurance meetings • Review and assess ongoing budget utilization and revenue recognition with Operations Managers to ensure projects are meeting financial targets • Manage internal CAT operations meetings and other trial-specific meetings, as appropriate • Significant contributor to multiple strategic departmental, sponsor-related and cross-functional initiatives • Participate in business development activities including; but not limited to proposals input, capabilities, and bid defense meetings • Apply thorough knowledge of industry regulations and guidelines to ensure operational compliance during clinical trial conduct