- Insmed Incorporated (NJ)
- …future of science , we're in. Are you?About the Role:The Global Regulatory Lead (GRL) will be responsible for formulating and implementing global regulatory ... contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive years, certification as… more
- Formation Bio (New York, NY)
- …area, business strategies, and the company's goals. About You BS, BSc, MS, MSc, PhD , PharmD, JD, or MD in science or healthcare preferred or equivalent ... to patients faster and more efficiently.About the PositionThe Senior Director, Regulatory Affairs lead is responsible for developing and directing the regional… more
- Eisai, Inc (WA)
- …imaging, genomics, proteomics, and precision medicine. Acting as the primary data science representative to global regulatory authorities, this individual will ... specifications and directions to the clinicians/statistical programmers. Supports the regulatory review and approval of the experimental therapies. May partner… more
- Eisai, Inc (Ann Arbor, MI)
- …mentoring, performance management and talent review. Ensure compliance with regulatory and other ethical guidelines relevant to the pharmaceutical industry, ... required and including international travel. Requirements Advanced scientific terminal degree (MD, PhD , PharmD) Must have a minimum of 5 years of experience within… more
- Eisai, Inc (Nutley, NJ)
- …difference. If this is your profile, we want to hear from you. The Medical Science Liaison (MSL or Sr. MSL) is a field-facing representative of US Medical Affairs ... Requirements: Advanced terminal D degree in medical or health sciences (eg MD/DO, PhD , PharmD) Experience: 2-3 years MSL experience in neurology or complex disease… more
- Legend Biotech USA, Inc. (Atlanta, GA)
- …the franchise.Fully understand and apply MSL SOP's/guidelines and company HCC/ Regulatory /Legal guidelines.RequirementsAdvanced terminal degree (PharmD, PhD , MD, ... the treatment of multiple myeloma.Legend Biotech is seeking Medical Science Liaison as part of the Medical Affairs team...part of the US Medical Affairs team, the Medical Science Liaison (MSL) will be responsible for engaging identified… more
- Merck & Co. (Rahway, NJ)
- …risks across all factors that may impact technical, operational & regulatory success or timelines. -Analyzes and develops innovative solutions to unforeseen ... circumstances.Responsible to ensure the best science and most robust processes are used, working closely with DCRC.- As the Product TPL takes ownership for the… more
- Merck & Co. (Rahway, NJ)
- …OR PhD in packaging/ mechanical/ chemical/ biochemical engineering, pharmaceutical science or chemistry or related fields with eight (8) years relevant ... substance and drug product container closure systems including mold qualification and regulatory compliance.- To act as master data stewards and support enterprise… more
- Merck & Co. (North Wales, PA)
- …Clinical Trials, Clinical Trials Analysis, Data Analysis, Data Management, Data Science , Numerical Analysis, Project Management, Regulatory Compliance, ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
- Merck & Co. (Rahway, NJ)
- …OR PhD in packaging, mechanical, chemical, biochemical engineering, pharmaceutical science or chemistry or related fields with eight (8) years of required ... and 3rd party logistics sites, supply chain and technology teams, and regulatory and project leaders. The successful candidate will demonstrate ownership and make… more
- Insmed Incorporated (NJ)
- …contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for four consecutive years, certification as ... Work list in the UK.For patients, for each other, and for the future of science , we're in. Are you?About the Role:We are seeking a highly experienced and visionary… more
- Merck & Co. (Rahway, NJ)
- …are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary function is to design, coordinate, monitor, and report clinical laboratory ... and field studies that will support the regulatory approval of new companion animal and livestock products. The position requires the candidate be responsible for… more
- Merck & Co. (South San Francisco, CA)
- …point in the drug development process, working closely with scientific, regulatory , statistical, and modelling colleagues across the organization to translate the ... benchtop science of preclinical discovery into compounds ready for assessment in large clinical populations.We are seeking a highly qualified physician-scientist… more
- Insmed Incorporated (NJ)
- …contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for four consecutive years, certification as ... Work list in the UK.For patients, for each other, and for the future of science , we're in. Are you?About the Role:We're looking for an Executive Medical Director of… more
- Merck & Co. (South San Francisco, CA)
- …and provide scientific leadership to guide decision-making.Stay current on emerging science , competitive landscape, and regulatory requirements in respiratory ... proactively addressed.Collaborate cross-functionally with medicinal chemistry, pharmacology, clinical, and regulatory teams to advance pipeline programs.Interpret complex data sets… more
- Insmed Incorporated (San Diego, CA)
- …contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive years, certification as ... list in the UK.For patients, for each other, and for the future of science , we're in. Are you?About the Role:We're looking for a Director, Clinical Scientist for… more
- Insmed Incorporated (NJ)
- …contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for four consecutive years, certification as ... patients, for each other, and for the future of science , we're in. Are you?About the Role:We are seeking...large molecules pipeline from preclinical through clinical development and regulatory approvals. In this role you will be a… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Genmab (NJ)
- …the CSRAttend operational and steering committee meetings, as applicableSupport regulatory submission/filing activitiesRequirementsMS / PhD or equivalent in ... compassionate, candid, and purposeful, and our business is innovative and rooted in science . We believe that being proudly authentic and determined to be our best… more
- Insmed Incorporated (NJ)
- …contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive years, certification as ... patients, for each other, and for the future of science , we're in. Are you?About the Role:The Associate Director,...coordination of MRC activities, compliance with company policies and regulatory standards, and the quality and integrity of all… more
