Alkermes

Job Description The Associate Director (AD), Medical Information & Review will participate in the medical review and approval of external communication materials, and provide accurate, scientifically balanced, and timely responses to inquiries from health care professionals, consumers, and other customers about Alkermes products. The AD will monitor the scientific literature and communicate new data to relevant internal groups, assist in the development of core medical information materials, and ensure medical accuracy of external communication materials related to Alkermes products. Candidates must take initiative and work independently with minimal supervision. Responsibilities Medical Information Independently research and write medical response documents and proactively update existing documents, obtain approval for use to ensure compliance with regulations and policies, and train others on their content and use. Receive, identify, document, and triage adverse events and...

Alkermes seeks an Associate Director in Medical Information & Review in Boston, MA. The role involves overseeing medical review and ensuring compliance with regulations while providing timely responses to inquiries regarding Alkermes products. The ideal candidate should have an advanced scientific degree and 3-5 years of experience in medical information, excellent communication skills, and the ability to work independently in a fast-paced environment. The annual salary is between $184,780 and $205,781, plus performance bonuses and benefits. #J-18808-Ljbffr

Job Description As a product and disease state expert within Medical Affairs, the Associate Director, Scientific Communications will provide medical, scientific and technical expertise to scientific communications deliverables for marketed and pipeline products. They will help develop, manage and track scientific communication plans as well as create and review deliverables for medical and scientific accuracy. The Associate Director will ensure compliance with Alkermes policies, procedures, and best-practices and support the development of key product materials for marketed and pipeline products. 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. Responsibilities Act as the Medical Communications lead for product-specific working groups or projects and support Publications, as needed Support other Scientific Communications Leads as...

The Associate Director, Medical Writing provides strategic and operational leadership for medical writing activities across one or more clinical development programs. This role combines hands‑on writing expertise with responsibilities for resource planning and matrix leadership to deliver high‑quality, fit‑for‑purpose clinical and regulatory documents aligned with program and regulatory objectives. The Associate Director is accountable for document development strategy, planning, and execution; leads clinical content development for complex submissions (including content strategy, organization, and resourcing); and partners with Clinical Development, Regulatory Affairs, Biostatistics, and other key functions to ensure cohesive messaging, mitigate risk, and support successful regulatory interactions and filings. The Associate Director applies advanced technical judgment to solve complex problems and ensures Medical Writing activities are integrated with broader development and...