Sr. Medical Director, Medical Affairs (Pipeline)

The Senior Medical Director for Pipeline is a highly visible and business-critical role that is part of the Medical Strategy team within Alkermes Medical Affairs. This role leads medical affairs efforts related to our early- and mid-stage development compounds. The Senior Medical Director for Pipeline will need to understand the business strategies and drivers underlying our emerging assets and translating those drivers into strategies and data generation and communication plans. The incumbent will need to effectively collaborate and communicate with colleagues within Medical Affairs, key cross-functional partners (e.g., New Product Planning, Clinical Development), and frequently represent the function and the company to senior management as well as with leading healthcare professionals.Why join Team Alkermes?Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.Highly motivated self-starter who can work independently, manage complex issues, and relate to multiple internal and external stakeholdersExperience working in a highly matrixed team environment and a demonstrated ability to lead through influence across the organization and at all vertical levels Proven record of problem solving, excellent communication skills (written and verbal), and experience interacting with and presenting to senior management and key external stakeholdersAdvanced degree in science or medicine required (e.g., MD, PhD, PharmD)Strong track record within the biopharmaceutical industry, with a minimum of 5 years’ experience Experience in Medical Affairs preferred Specialized training or experience in neurology or psychiatry preferredExperience with peer-reviewed publications Strong scientific background, creativity, flexibilityWorking knowledge of regulatory and compliance requirements Other:Willingness/ability to travel up to 25%, with both domestic and international travel expectedThis role is preferred Hybrid (3 days per week in office)Alkermes has recently adopted a hybrid working environment to support and meet the needs of employees and this role will operate in a flexible environment with 60% of time in the office and 40% from home. This position is eligible for the hybrid workplace model, requiring work to be completed onsite at our Waltham, MA office at least 3 days per week. This role is not eligible for fully remote work. The annual base salary for this position ranges from $290,000 to $340,000. In addition, this position is eligible for an annual performance pay bonus. Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package. Additional details can be found on our careers website: #LI-MB1Contribute to the identification of therapeutic areas to pursue with our pipeline agents based on mechanism of action, pathophysiology, unmet need, and other considerationsContribute strategic input into the design and selection of endpoints to be included in clinical trialsDevelop and maintain an in-depth awareness of the evolving treatment landscape, therapeutic area trends, pharmaceutical/biotech company pipelines, and the evolving payer landscape and communication needs across disease areas of focus for Alkermes’ pipeline assetsAnalyze and interpret scientific data, disease/treatment landscape, and external stakeholder evidence to identify challenges, opportunities, and strategic imperatives to communicate and demonstrate our portfolio value Foster relationships with and solicit input from key medical opinion leaders, researchers, and relevant medical societies and patient advocacy organizationsCollaborate with Health Outcomes Research and Patient Advocacy to represent the patient voice in our clinical development activities Provide medical and scientific training and/or support to other staff across functionsLead the medical affairs strategic planning process for our pipeline assets and ensure strategic alignment of medical plans to Alkermes’ programmatic goals and objectives. Ensure execution of medical tactics associated with the strategic plan(s)Guide the scientific and medical communication planning process. Review and approve scientific publications, investigator-initiated study proposals, medical education grant initiatives, corporate communications and othersFull timePosting Date: 2026-05-06