Primary leadership role for clinical development strategy, protocol design across all clinical research trials in all projects across neurology. Direct authorship contributions in protocols, clinical study reports, and publications Lead and develop clinical development staff and oversee hiring of additional staff as needed. Interact with senior management and serve as a s

Lead and manage clinical pharmacology, DMPK, and bioanalytical sciences groups and assume a role of "subject matter expert" within the fields. Provide leadership and scientific oversight in designing and interpreting data from early stage development clinical studies and on occasion act as a study lead on clinical pharmacology studies Draft and provide guidance to other j

Identify and map influence in state and regional ecosystems Develop and deploy KOL engagement strategy Oversee VIVITROL Speakers Program Design VIVITROL Conference/NGO Plan Partner with Sales to develop district / state level market development strategies Manage KOL consultants Manage marketing ad boards Maintain regular communication with Field Sales and sales management

Alkermes, Inc. is the U.S. operating company of Alkermes plc, a fully integrated, global biopharmaceutical company that applies its scientific expertise and proprietary technologies to research, develop and commercialize, both with partners and on its own, pharmaceutical products that are designed to address unmet medical needs of patients in major therapeutic areas. Alke

Develop and execute public sector and managed care payer strategies for targeted regional plans to secure coverage for newly marketed products, minimize barriers to access, solve reimbursement issues, and support sales for Alkermes marketed products Work within a cross functional team focusing on Alkermes' core classes of trade Commercial Managed Care (Regional Plans) Med

Develop and execute public sector and managed care payer strategies for targeted regional plans to secure coverage for newly marketed products, minimize barriers to access, solve reimbursement issues, and support sales for Alkermes marketed products Work within a cross functional team focusing on Alkermes' core classes of trade Commercial Managed Care (Regional Plans) Med

Demonstrate a subject matter expert role in coordination of Alkermes product education and account management, product education for large treatment systems, aligning the resources and capabilities of internal cross functional teams Actively lead field partners to maximize the growth of local MAT treatment programs by developing a deep understanding of assigned geography,

Maintain corporate governance documents and records, including board and committee minutes, consents and other corporate filings Manage director and officer information and assist with Board communications, including preparation and distribution of materials for Board and committee meetings and coordination of committee calendars Prepare for annual meeting of shareholders

The Senior Clinical Programmer is responsible for clinical programming activities to support data management, data cleaning, data review and surveillance reporting activities for global projects, as well as management of external data specifications, reconciliation programming and effective oversight of external data vendors in partnership with the Data Management Lead. E

Alkermes is searching for a highly talented Scientist responsible for developing and evaluating cutting edge technologies and concepts for protein modeling and engineering. The newly designed proteins are expected to be the first or best in class biologics to support early drug discovery in multiple disease areas, including oncology, immunology, fibrosis and others. KEY D

Alkermes is seeking a highly motivated and talented scientist to join the in vitro CNS team to support drug discovery. This is an exciting bench focused position and the candidate will contribute to various projects from target validation, lead compound optimization to clinical candidate selection to drive therapeutic programs forward. The candidate should have a track re

Alkermes, Inc. is the U.S. operating company of Alkermes plc, a fully integrated, global biopharmaceutical company that applies its scientific expertise and proprietary technologies to research, develop and commercialize, both with partners and on its own, pharmaceutical products that are designed to address unmet medical needs of patients in major therapeutic areas. Alke

Alkermes is seeking an experienced individual responsible for supporting the daily manufacturing and facility operations, along with project support. Functions include proactive support of change control assessments, documentation reviews and validation review/support. Functions also include reactive support of discrepancy identification and resolution on the floor, Inves

Serve as strategic business partner to the product team Serve on the review committees for promotional materials and medical materials Provide legal counsel to commercial organization, including in respect of commercial program design, implementation and compliance with Federal and state anti kickback statutes, false claims acts, the Food, Drug and Cosmetic Act, HIPAA, pr

Leadership of Quality Assurance, Quality Control and Validation functions across the Wilmington Ohio site. Ensure that Wilmington as well as the third party Supplier sites operate in compliance with FDA and EU and all other regulations, as required by our Quality Systems and our Quality culture, to be inspection ready always. Interface with FDA, DEA and any other regulato