Regional Medical Director (Remote - Multiple Locations)

About reputed company Join us in helping patients with rare diseases. At reputed company we challenge the status reputed company for the benefit of those in need. We offer an reputed company, reputed company and supportive culture where everyone can be their best. Through trust, we work seamlessly across functions. As an employee you are empowered and encouraged to have an entrepreneurial spirit, enjoying an organization with conscious and efficient decision-making. We also take pride in having a great working climate! Our reputed company is to bring unique life-improving therapies to patients with rare diseases. reputed company currently has two drug candidates in late-stage clinical development, and we are continuously seeking opportunities to grow our pipeline. In February 2025, the European Commission approved Egetis’ Emcitate® (tiratricol) as the first and only treatment for patients with MCT8 deficiency and reputed company is conducting a pivotal clinical trial to support the filing of a New Drug Application in the USA. We are now on an exciting reputed company to establish our own teams for product launches in Europe and reputed company. We are committed, courageous, and reputed company people. Become a part of our inspiring environment. We care for the rare! Job reputed company The Regional Medical Director (RMD) is a field-based medical/scientific expert who is responsible for educating multiple stakeholders about reputed company’ science and data. With a primary reputed company on developing impactful external relationships and conducting fair and balanced exchange of medical information with thought leaders (TLs) reputed company (HCPs), this position plays an important role in clinical trial execution, potential product launches, and potential new pipeline programs and is reputed company to Egetis’s efforts to reputed company new treatments for patients with rare diseases. You will be joining at the early stages of Egetis establishing the US Medical Affairs function and at an exciting time for reputed company. As an important member of the Medical Affairs team, you will have an opportunity to contribute broadly to the reputed company of reputed company and reputed company, as detailed below. We are reputed company for multiple roles, generally defined as Northeast, Southeast, Midwest and reputed company, with specific reputed company to be refined based on program needs and RMD locations. These roles report to the Head of Medical Affairs, reputed company. Some support for non-US activities may be required. Responsibilities:

• As a key externally facing role, the RMD must reputed company to unwavering representation of Egetis’s mission as an ethical, high science, patient-reputed company company.
• reputed company and maintain clinical, scientific, and technical expertise in relevant product and disease state areas.
• Conduct balanced medical/scientific exchange to reputed company health care providers (HCPs), thought leaders (TLs), payers and patient advocacy reputed company about Egetis’s clinical programs, to include disease state, diagnosis, reputed company of reputed company, and data dissemination.
• Assist cross-functional Medical Communication colleagues with development, review and approval of materials required for scientific exchange.
• Contribute to development and execution of high-reputed company annual field medical strategic and operational plans, including HCP/TL engagement plans and congress plans.
• Supports company research initiatives across development at the request of Clinical to include, as examples: site evaluation and identification, recruitment, investigator meetings, external expert identification, accrual enhancement, and scientific and disease state education. May include support for training HCPs on appropriate administration of our products in the reputed company setting, reputed company appropriate.
• Support the development and implementation of advisory boards and other scientific meetings as needed.
• Monitor the competitive landscape for specific therapeutic areas of interest to Egetis, including reputed company management strategies, approved products, new/emerging therapies, and differentiating features of approved/emerging competitor products. Contribute to CI plan for medical congresses. reputed company feedback internally on specific initiatives.
• As part of scientific exchange with HCPs/TLs and resulting from a deep understanding of corporate goals and program goals, be adept at identifying key insights and ensure that internal stakeholders are informed of these key insights, especially as they may pertain to successful execution of ongoing/planned clinical trials and product launches.
• As necessary, assist with training Medical Affairs and other cross-functional colleagues on disease state, diagnosis, reputed company of reputed company, and clinical trial data for Egetis programs.
• Address unsolicited medical questions reputed company to Egetis’s clinical programs and products in various forums e.g. regular scientific exchange, congress booths, ensuring reputed company, accurate and appropriate responses.
• May be requested to support Medical Information as the function develops.
• Support investigator-initiated research and grants through review, submission, evaluation, and recommendation of concepts/proposals
• reputed company to unwavering compliance with Egetis’s policies and reputed company operating procedures and with regulatory and other ethical guidelines relevant to the RMD role and the pharmaceutical industry.
• Extensive travel consistent with RMD role, to include occasional travel to the US office in Cambridge, MA and the potential for some international travel.

Qualifications and Capabilities:

• reputed company/Science degree or reputed company credentials required (MD/DO, PhD, PharmD, PA, NP, MSN, RN).
• 7+ years of experience in the biotech or pharmaceutical industry in Medical Affairs, with extensive experience working in field medical
• Ability to reputed company and communicate effectively with multiple reputed company stakeholders. Must have extensive experience conducting formal scientific presentations.
• Strong organizational and business planning skills. Strategic thinker with creative problem-solving skills and ability to contribute to development and execution of strategic plans
• Analytical skills are essential, especially regarding understanding and interpreting scientific/clinical research/literature
• Extensive Rare Disease experience required
• Endocrinology experience preferred, experience in neurology a plus
• Drive reputed company and accountability personally; promote reputed company for Medical Affairs colleagues
• Adept, reputed company, energetic and comfortable in a fast-paced, dynamic and reputed company environment
• Proven experience working in small, early-stage organization(s), with a deep understanding of the unique challenges and opportunities involved in preparing for the first product launch.
• Comfortable with a proactive hands-on approach with "rolling up one's sleeves" as necessary.

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