Director, Scientific Communication and Operations, Medical Affairs

Who we are:Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston’s top workplaces for the past several years.How we work:PIONEER: We are courageous, resilient and rigorous in our mission to improve patients’ lives through our revolutionary degrader medicines.COLLABORATE: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.How you’ll make an impact:The Director Scientific Communication and Operations, Medical Affairs, reporting into the Vice President, Medical Affairs, is a strategic leader responsible for developing and executing Medical Affairs strategy across Medical Affairs Scientific Communications and Operations, spanning data generation and dissemination, scientific publications, medical-to-medical content development, and field medical training materials, as well as operational planning, congress planning, grants and sponsorships, cross-functional coordination, and advisory boards. This role will work cross-functionally with internal stakeholders (R&D, Commercial, Regulatory, etc.) and externally with healthcare professionals, key opinion leaders (KOLs), and scientific organizations to ensure impactful and compliant medical engagement and education aligned with corporate objectives.Drive the creation and implementation of a highly scientific and compelling scientific strategy across manuscripts, abstracts, and posters, aligned with the company's clinical and educational objectives.Develop and implement Kymera’s scientific strategy and medical presence at major congresses, including logistics, medical booth materials, symposia, data presentations, and cross-functional deliverables.Review, interpret, and translate clinical data into accurate, compelling scientific narratives for internal and external audiences and drive impactful initiatives.Lead the development of medical-to-medical content and medical information, including scientific platforms, lexicons, and educational materials, ensuring accuracy, scientific rigor, and regulatory compliance.In collaboration with the field medical team, create and maintain field medical training and scientific education materials to enhance scientific knowledge across the organization and among healthcare providers.Lead operational planning and execution across Medical Affairs, including budgeting, timelines, and the management of third-party vendors.Oversee the review, approval, tracking, and compliant execution of medical education grants, sponsorships, and collaborations with external scientific organizations.Drive cross-functional coordination with R&D, Commercial, Regulatory, and external agencies to ensure seamless delivery of logistics and deliverables across Medical Affairs functions.Manage advisory boards including planning, coordination with internal colleagues, agency management, FMV process, and KOL contracting.Skills and experience you’ll bring:Advanced degree (MD, PharmD, PhD) in a scientific or clinical discipline required. Immunology experience strongly preferred. Minimum 7+ years of experience in Medical Affairs roles within the pharmaceutical or biotech industry.Proven track record developing and driving impactful Medical Affairs data generation, dissemination, and scientific publication strategies based on clinical trial data, market dynamics, corporate objectives, and healthcare provider educational needs.Clear understanding of clinical research methodologies and ability to independently evaluate and translate scientific material in an effective, credible manner.Strong business acumen and understanding of immunology/inflammation market dynamics and key value drivers.Knowledge of latest digital channels/tools to optimize education of and interactions with healthcare providers, advocacy organizations, patients, and key partners.Direct knowledge of promotional regulatory processes, Fair Market Value (FMV) process, tiering, and alignment with third-party vendors.Experience managing scientific congress logistics and advisory board operations, including budgeting and vendor oversight.In-depth knowledge of compliance, regulatory, and industry standards.Exceptional leadership, project management, and strategic thinking abilities.Excellent communication, presentation, and interpersonal skills.Equal Employment OpportunityKymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.CompensationKymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.The anticipated base salary range for this role is $195,000 – $275,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate’s depth of experience and the capabilities they bring to the position.