Job Description

Medical Director, Global Medical Affairs at Lonvo-z Apply locations: Cambridge, MA Time type: Full time Posted on: Posted 30+ Days Ago Job requisition id: R1124 Why Join Intellia? Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases. We live our four core values: One, Explore, Disrupt, Deliver. We believe in curiosity, pushing boundaries, and developing innovative solutions. Patients depend on us to turn our promises into reality, so we maintain high standards and focus on results. We encourage our people to go beyond what is possible. We aim to cure, motivated by change and the possibilities of what we can achieve together. Role Overview As Medical Director for the Lonvoguran Ziclumeran program, you will create innovative US and global Medical Affairs strategies to support Intellias CRISPR/Cas9 programs. The ideal candidate has clinical and pharmaceutical industry experience, especially in rare diseases and product launches. You will align commercial and medical goals, develop medical content in collaboration with the Scientific Communication team, and serve as the medical expert on regulatory and review committees. Responsibilities Ensure content appropriateness aligning with strategy and narrative, collaborating across Medical Affairs functions. Identify and develop data and publication content; lead medical symposiums. Guarantee medical accuracy and balanced information in educational and communication materials. Collaborate with Scientific Communications to ensure publications meet medical strategy and target audiences. Obtain review and approval of materials for field teams. Work with Medical Lead, Patient Advocacy, Scientific Communications, and Field Medical to execute external engagement strategies, including advisory boards. Propose and design studies for post-marketing evidence generation, including observational and real-world studies. Coordinate with Access & HEOR to support educational and engagement initiatives. Partner with Commercial to ensure medical accuracy in messaging and campaigns. Participate in congresses, develop content, and present at medical education programs. Serve as a medical SME in cross-functional training. Requirements Skills & Abilities Experience with medical/promotional content review committees. Strong communication, strategic, interpersonal, and negotiation skills. Ability to work independently and execute projects. Experience analyzing clinical trial data and designing real-world evidence studies. Product launch experience preferred. Research experience in relevant therapeutic areas preferred. Knowledge of field team material needs and medical information. Diplomacy, positive influence, and conflict management skills. Ability to work in a fast-paced, matrixed organization with multiple stakeholders. Education & Experience Doctorate Degree (MD, PhD, PharmD) with at least 7 years in Medical Affairs within biotech/pharma, including leadership in product launches. Physical & Other Requirements Ability to sit or stand for hours, manual dexterity, and quarterly travel. Covid-19 vaccination is strongly encouraged. About Us At Intellia, we aim to make CRISPR/Cas9-based medicines a reality for genetic diseases and develop engineered cell therapies for immuno-oncology and autoimmune diseases. #J-18808-Ljbffr

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Full time,

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