- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a QC Data Reviewer as part of the Quality team based in Raritan, NJ. Role Overview The ... QC Data Reviewer is an exempt level position responsible for reviewing...in a controlled GMP environment. Key Responsibilities Perform peer review /approval of laboratory data including but not limited to… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …treatment of multiple myeloma. Legend Biotech is seeking a Lead QC Microbiology Data Reviewer as part of the Quality team based in Raritan, New Jersey. Role Overview ... The Lead QC Microbiology Data Reviewer is an exempt level position with responsibilities for...commercial operations in a controlled cGMP cleanroom environment. Create, review and approve relevant QC documents, logbooks, SOP's and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Depending on the status of development of the compound, lead and medical -scientifically direct a team of junior physicians and scientists responsible for 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 ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… 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 ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …allocation, budget allocation, and assessment of needs including training, data review tools, etc.Standing PRG reviewer for mid-to-late-stage asset protocolsCore ... documents (writing of ICF, DM charter, response assessment charter, etc), clinical data review excellence with a focus on patient safety and data integrity, site… more
- BioAgilytix (Boston, MA)
- …II/III will perform responsibilities of a traditional lab analyst, peer reviewer , and new system implementation specialist. Tasks will encompass running assays, ... analysis projectsTroubleshoot assaysCompile/process data (make power export)Prepare summary tablesPeer review raw dataOrder reagentsParticipate in assay development and validationResponsible… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... compliant with regulatory requirements, including CDISC ADaM data set specifications, reviewer 's guides, etc- Global Biostatistics Data Management (BDM) Strategy to… more
- Eisai, Inc (Nutley, NJ)
- …internal business processes including leading and/or active participation in relevant medical review committees.Partner with key internal stakeholders to support ... At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides...Phase IV clinical development programs for assigned products.Design and review IIS strategies and review proposals in… more
- Merck & Co. (North Wales, PA)
- …inquiries, handling of escalated complex global HCP inquiries, and insight generation/analysis), Medical Review of US and HQ-created global Promotional Materials ... US and international congresses to verbally answer unsolicited inquiries from HCPs.Scientific/ Medical Review of US and Global Promotional and Non-Promotional… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... with a high degree of quality in the execution of all Global Oncology Medical Affairs (GOMA) Company Sponsored Studies (CSS) and Medical Access/Expanded Access… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... compliant with regulatory requirements, including CDISC ADaM data set specifications, reviewer 's guides, etc.- Global Biostatistics Data Management (BDM) Strategy to… more
- Eisai, Inc (Nutley, NJ)
- At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... and make a difference. If this is your profile, we want to hear from you.The Medical Director, US Medical Affairs provides medical leadership for medical … more
- Eisai, Inc (Nutley, NJ)
- At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... If this is your profile, we want to hear from you. Job Summary The Medical Director will provide medical leadership for medical affairs strategy, planning… more
- Eisai, Inc (NJ)
- At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... is your profile, we want to hear from you. Job Summary The Senior Manager, Medical Writing will be the designated Lead Medical Writer for approximately 3-4… 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 ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Gains strategic and planning alignment across regions and functions, and supports review of local country/regional Medical Affairs activities when applicable. ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Novo Nordisk Inc. (Milwaukee, WI)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Taiho Oncology (New York, NY)
- Sr. Medical Science Liaison New Jersey, USA New York, NY, USA Philadelphia, PA, USA Req #372 Monday, May 20, 2024 Looking for a chance to make a meaningful ... us. Field-Based Employee Value Proposition: Exciting opportunity to join a team of Medical Science Liaisons and collaborate with a dynamic and growing Medical … more
- Taiho Oncology (TX)
- Medical Science Liaison Texas, USA Virtual Req #330 Tuesday, May 7, 2024 Looking for a chance to make a real difference in the oncology space? Taiho Oncology is on a ... Territory Coverage: South Central - TX, AR, LA, and OK Position Summary: The Medical Science Liaison (MSL) is a field-facing representative of the Medical … more
