- Merck & Co. (South San Francisco, CA)
- …Education: Master's in biology, pharmacology, medicine or related fields with four (4) years of relevant experience listed below Ph.D. or MD in biology, pharmacology, ... medicine or related fields with two (2) years of relevant experience listed below Required Experience and Skills: Strong writing skills and experience drafting study reports, scientific manuscripts, or scientific documents Experience with laboratory operations… more
- Ochsner Health System (Harvey, LA)
- …Duties Assesses, designs, presents and provides evaluation of educational program for clinical and non - clinical staff based on identified needs/competencies. ... Actively participates in groups and professional associations. Functions as a performance consultant. Coordinates training facilities and other resources. Other related duties as required. The above statements describe the general nature and level of the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with commercial group regarding new indications for Life Cycle Management.Additional non -study related activities: Clinical Development involvement in due ... immune disorders. Summary Drafts development plans, protocol profile, protocol, and clinical sections of submission documents under guidance of CSL and/or Medical… more
- Merck & Co. (Rahway, NJ)
- …technical or other potential problems arising in the design, conduct, and analysis of non - clinical or clinical studies, proposes solutions and carries them ... / vaccine discovery and development programs.Analyzes data and interprets results from non - clinical or clinical studies.--Applies and implements basic and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Coast Development Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Non - ... as a member of the first safety committee chaired by non - clinical , where Safety Surveillance will resume chairmanship going forward Establish, operate… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Coast Development Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Non - ... as a member of the first safety committee chaired by non - clinical , where Safety Surveillance will resume chairmanship going forward Establish, operate… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Coast Development Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Non - ... Participate as a member of the first safety committee chaired by non - clinical , where Safety Surveillance will resume chairmanship going forward. o Establish,… more
- Merck & Co. (Rahway, NJ)
- …and partnering for Pharmaceutical development/ CMC with Quality, Regulatory, Operations, Non - clinical , Clinical , and other functional areasExperience with ... proteins as well as the biopharmaceutic support for the oral and non -oral portfolio. Within Biologics and Biopharmaceutics, the large molecule product development… more
- Insmed Incorporated (San Diego, CA)
- …full development status. They will collaborate with R&D and may assist with non - clinical biomarker quantification and testing efforts to ensure an appropriate ... MS/MS or equivalent systemsMay serve as a liaison with R&D for non - clinical / clinical biomarker LC-MS related needs.Serve as a subject-matter-expert for all… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders. Summary Oversees typically a single non -pivotal trial (small size, standard complexity in design and geographic scope). ... Prepares clinical section of regulatory document. Collaborates as team member...Establishes effective communication between CRO / vendors / AROAdditional non -study related activities: Occasional senior management interactions at FIHC,… 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 ... effective execution of CMR foundational and role-specific/technical training (eg clinical trial-related, GxP, Compliance, etc.) across the US and...the US and Canada as well as support the CMR/ non -CMR activities in Mexico City GBS and East Coast… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …is responsible for the ownership and management of these processes for GxP and Non -GxP systems and services. In this position, the GSM will lead major incident ... calls, conduct problem management meetings, and drive process and policy adaptation within the support teams and across business units. The GSM is responsible for the training, performance tracking, and reporting of these processes, and works across all… more
- Amsterdam Nursing Home (Woodside, NY)
- …rate is $35.38 with an additional 10% shift differential for evening and nights Non -Union $45/hr. We just raised our rates! $2,000 Sign-On Bonus for FULL-TIME!! NEW ... combination of old-world charm, comfortable surroundings, and a state of the art clinical care. Our longstanding tradition of caring is carried out by an exceptional… more
- Novo Nordisk Inc. (Philadelphia, PA)
- …assess, create and maintain advocacy of customers aligned to company, brand and clinical goals. The OCS develops local strategies and executes local tactical plans ... partners. The OCS also assists their customers with their local clinical and educational initiatives by coordinating company resources (eg, counterparts, materials,… 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 ... Medical Affairs, Medical Strategy & Operations, Medical Information, Publications, Clinical Directors, HEOR Directors, Global Medical Directors, Marketing, and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …such as: different approaches to data review in conjunction with Data Management and Clinical Science, audit trail review for non -logical timing of entry and/or ... a Quality by Design (QbD) and Risk-Based Quality Management (RBQM) approach to clinical trial conduct. Major focus is on operations concerning risk control and… more
- Merck & Co. (Rahway, NJ)
- …programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into ... or related field plus 9 years SAS/R programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …oversight over the site Quality Control laboratories responsible for testing of pre- clinical , clinical , and commercial stage CAR-T cellular therapy products. ... providing quality oversight for site Quality Control laboratories responsible for testing pre- clinical and clinical and commercial stage CAR-T cellular therapy… 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 procedures. Relationships This position reports to a Senior Director within the Clinical Data Science & Evidence (CDSE) - RWE team. This role will interact… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of the manufacturing facility utilized for cell therapy products for clinical trials and commercial operations in a controlled GMP environment.Key Responsibilities ... Responsible for performing routine EM sampling, including viable/ non -viable air and surface sampling, related to the manufacturing of autologous CAR-T products for … more
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