Medical Science Director

Medical Science Director

If you are interested in joining an entrepreneurial team, focused on bringing life-saving therapies to market for critical unmet medical needs, consider applying for a role at CorMedix Therapeutics. The culture at CorMedix Therapeutics is patient-centered where we feel a sense of urgency to solve some of the most pressing issues in hospital-based healthcare.

CorMedix Therapeutics's greatest asset is our people. We have a deeply experienced team and continue to bring on some of the brightest talent that can problem solve and execute with high-precision. We are passionate about the work we do and how we do it. We believe in building highly engaged teams that exude integrity, open communication, and innovation. We believe in fostering each employee to reach their highest potential by offering an inclusive environment, opportunities to challenge yourself and grow, and a community of purpose. We expect that everyone here brings their best selves to work and together, our singular efforts culminate into profound and meaningful breakthroughs.

CorMedix Therapeutics is a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of life-threatening conditions and diseases in the United States. CorMedix is focused on selling and marketing products in institutional settings of care in the US and has field based medical and commercial infrastructure deployed in hospitals, clinics and infusion centers. Rezafungin is currently approved for the treatment of candidemia and invasive candidiasis in adults.

The Medical Science Director (MSD) is a field-based scientific professional responsible for supporting medical affairs activities across oncology, infectious disease, nephrology, acute care, and related therapeutic areas through compliant scientific exchange, insight gathering, and cross-functional collaboration. The MSD serves as a scientific resource to healthcare providers (HCPs), key opinion leaders (KOLs), pharmacy stakeholders, and institutional decision-makers across inpatient and outpatient healthcare settings. This role supports both commercialized and pipeline products through clinical engagement, medical education, evidence communication, and healthcare ecosystem collaboration.

The MSD will contribute to medical affairs initiatives by identifying and communicating clinical insights, supporting evidence generation activities, and helping facilitate effective scientific engagement across healthcare systems and treatment settings.

Location Requirement: This is a field-based position supporting a multi-state territory that currently includes Virginia, North Carolina, South Carolina, and West Virginia. Candidates must reside within the territory. Preference will be given to candidates located in Virginia, North Carolina, or South Carolina or in locations that provide efficient access to major healthcare systems and regional travel hubs within the territory. The selected candidate must be able to travel extensively throughout the territory (approximately 60–70%) and attend customer meetings, scientific conferences, and other business-related events as required.

Primary Responsibilities:

• Identify and engage emerging and established KOLs across oncology, including Bone Marrow Transplant (BMT), infectious disease, nephrology, critical care, antimicrobial stewardship, and related therapeutic areas, while serving as a trusted scientific and clinical resource to HCPs, pharmacy leaders, infection prevention specialists, and healthcare systems.
• Conduct compliant, fair-balanced scientific exchange regarding clinical data, disease states, and pipeline programs.
• Develop and maintain relationships with clinical decision-makers and institutional stakeholders within acute care, oncology, and hospital systems.
• Support scientific discussions at medical congresses, advisory boards, symposia, and professional society meetings.
• Facilitate peer-to-peer educational opportunities addressing unmet clinical needs and treatment challenges.

• Capture and communicate medical insights, competitive intelligence, treatment landscape trends, and unmet needs to internal stakeholders.
• Contribute to the development and execution of medical affairs strategy, including publication planning and evidence dissemination initiatives.
• Support internal cross-functional teams including Clinical Development, Commercial, HEOR, Market Access, Pharmacovigilance, and Medical Information.
• Provide scientific input into educational materials, strategic initiatives, and field medical planning activities.

• Identify potential clinical trial sites, investigators, and referral networks to support enrollment and study execution.
• Educate investigators and healthcare providers on clinical trial protocols and scientific rationale.
• Support investigator-sponsored research initiatives and collaborative research opportunities where appropriate.
• Assist in identifying barriers to product adoption and help develop evidence-based clinical solutions.

• Respond appropriately to unsolicited medical information requests in accordance with corporate compliance policies and regulatory guidelines.
• Document and communicate adverse events and product complaints according to pharmacovigilance procedures.
• Maintain expertise in relevant disease states, products, competitors, clinical literature, and regulatory standards.

• Provide scientific education and training to internal stakeholders.
• Collaborate effectively within a matrix organization to drive aligned medical objectives.
• Contribute to a high-performance, patient-focused, and collaborative team environment.

Qualifications & Experience:

• Advanced healthcare or scientific degree required (MD, DO, PharmD, PhD, DNP, NP, PA-C, or equivalent).
• Prior field medical/MSD/MSL experience preferred, including 1+ years of MSL or equivalent scientific engagement experience preferred.
• 1–5+ years of experience within an academic institution, healthcare system, pharmaceutical, biotech, or related industry setting preferred.
• Oncology experience required, including experience in Bone Marrow Transplant (BMT).
• Experience within infectious disease, nephrology, critical care, acute care, or supportive oncology strongly preferred.
• Experience supporting hospital-based specialty products preferred.
• Demonstrated ability to engage healthcare systems, institutional stakeholders, and key opinion leaders.
• Clinical-stage and/or commercial-stage experience preferred.
• Experience with scientific exchange, evidence communication, and medical education activities preferred.
• Experience working in fast-paced or emerging biotech environments preferred.

Skills & Requirements:

• Exceptional scientific communication and presentation skills.
• Strong relationship-building capabilities with healthcare providers, institutional stakeholders, and key opinion leaders.
• Ability to interpret and effectively communicate complex clinical and scientific information.
• Demonstrated cross-functional collaboration and teamwork within matrix organizations.
• Strong organizational, analytical, and problem-solving skills.
• Ability to operate independently and manage multiple priorities effectively.
• High level of professionalism, integrity, sound judgment, and compliance orientation.
• Proficiency with scientific literature evaluation, medical data interpretation, and insight gathering.

Position Type / Expected Hours of Work:

Full Time

Travel Requirement:

• Field-based position with significant travel required (approximately 60–70%).
• Ability to travel overnight and attend scientific conferences and customer meetings.

EEO Statement:

CorMedix is an equal opportunity employer. The Company is committed to providing a safe, respectful, and professional work environment that is free from all forms of unlawful discrimination, harassment (including sexual harassment), and retaliation, and complies with all applicable laws prohibiting such conduct. CorMedix does not discriminate against any individual on the basis of race, religion, color, national origin, ancestry, sex, marital/civil union/domestic partner status, family or parental status, sexual orientation, age, disability, or any other status protected under applicable federal, state, or local law.