As a synthetic chemist have the ability to drive compound design through the utilization of synthetic expertise for a given project directed toward successful project progression and candidate drug delivery Design and safely perform experiments, working independently as well as part of a team, propose synthetic routes for new analogs Ensure robust synthetic routes for all

The Manager or Associate Director of Biostatistics will support drug development activities and decision making encompassing Phase I IV studies. This includes guidance on designing studies, selecting appropriate and innovative statistical methods, analyses, interpretation, and reporting of study results. Duties and Responsibilities Work with a group of biostatisticians to

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 a Senior Technical Systems Analyst to join our Information Technology Project Delivery (Build) Team. Core principles of the required skillset are the ability to work in ambiguous solutions, interacting with end users and a strong sense of ownership . This role will be involved in systems and solutions cross the entire business area with a focus on Rese

Drug Safety Epidemiology is a function within Alkermes supporting Drug Safety activities and clinical development programs across the product life cycle. The primary purpose of the Associate Director role is to lead all epidemiology support activities within multiple therapeutic areas, to manage various epidemiology projects led by DSPV, and to manage and mentor direct re

Prepare and process monthly general ledger journal entries; including, but not limited to fixed assets, intercompany settlements, prepaid expenses, month end accruals, and other miscellaneous entries. Participate in the month end closing procedures; including the reconciliation of asset, liability, equity and expense accounts Responsible for monthly expense account analys

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

This is a temporary position. Temp QC Analyst II The QC Analyst II will join chemistry group to perform analytical testing, instrument qualification as required to meet QC cycle times following cGMP. Responsibilities will also include reviewing, reporting test results and ensuring that all activities within the laboratory are performed in compliance with cGMP, internal wr

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

The QC Analyst must be a competent professional who is able to network with internal colleagues and external vendor representatives, consultants and other professionals. Using this network and their own experience and expertise, they are able to develop creative and compliant solutions to challenges. They must be familiar with the common techniques and equipment within a

This position will execute the development of novel active pharmaceutical ingredients (API) within the immuno oncology biologics pipeline from the early Process Development stage through GMP production (Clinical Phase 1 3). The candidate will join a diverse and dynamic team of experienced scientists and engineers in a brand new lab space. The candidate will support intern

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

In this position, you will be expected to independently review, prepare and negotiate a high volume of a life sciences agreements of relative complexity, including master service agreements, clinical trial agreements, consulting agreements, confidentiality agreements, license agreements, termination notices, amendments, among others. Collaborate and communicate closely an

The QC Analyst I will be responsible for performing functions including environmental monitoring, utilities monitoring, and testing in a facility that manufactures sterile products and tablets in a GMP environment. The hours are Monday Friday, 12 00am 8 30am. Major Responsibilities Perform environmental monitoring in aseptic, classified, and controlled areas (routine, bat

Performs Level 2+ support for applications and system in the laboratories. Issues may span network, desktop, and laboratory equipment. Duties include User account management System administration duties Configuration, queries, and report development Ensures accuracy and completeness of data, provides resolution to issues identified and updates procedures. Ensures and main