- Novo Nordisk Inc. (Los Angeles, CA)
- …rights and wellbeing; data reliability; scientific integrity; regulatory and process compliance ) for monitoring and site management activities. Takes ownership ... for NACD and Novo Nordisk (eg, clinical trial site staff, clinical research vendors). Manages relationships with multiple internal stakeholders relevant to the… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Functions Oversee performance of CROs, third party vendors, and contractors, including co- monitoring , to ensure compliance with study protocol, and identifying ... in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Experience:10 or More Years of related pharmaceutical industry or Clinical Research Organization experience required4 or More Years monitoring experience ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: This… more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the planning and directing clinical research activities within the Atherosclerosis and Metabolism therapeutic area, with a ... the entire cycle of clinical development, including study design, placement, monitoring , analysis, regulatory reporting, and publication. - Specifically, the Senior… more
- Merck & Co. (Rahway, NJ)
- …Clinical Development, has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs in the Oncology Clinical ... Research group and in the field of Thoracic Oncology...clinical development, including development strategy, study design, initiation, execution, monitoring , analysis, regulatory reporting, publication, and presentation at national… more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our company's ... entire cycle of clinical development, including study design, placement, monitoring , analysis, regulatory reporting, and publication.Specifically, The Senior Director… more
- Aequor (South San Francisco, CA)
- …and commitment to animal welfare.Ideal candidate: Strong background in in vivo research techniques with hands-on experience handling rodents in a professional lab or ... surgical procedures, in vivo imaging, mini pump implantation, and post-procedure monitoring , is highly desirable. Strong written and verbal communication skills,… more
- Merck & Co. (Rahway, NJ)
- …and methods of pharmaceutical research , participate in the writing of research protocols, conduct of clinical trials, safety monitoring , analysis of data ... health agencies (eg FDA); understand key elements in pharmacovigilance, drug safety monitoring , signal detection and processing of adverse reports After a successful… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …team and the Monitoring and Investigations teams. This includes writing and research assignments under the direction of various Compliance functions as well ... providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders....diseases and immune disorders. We are currently seeking a Compliance Intern for the year (June 2025 - May… more
- Merck & Co. (Durham, NC)
- …activities requiring support include the process and technology introduction, compliance improvements, and manufacturing readiness to initiate production of ... assignments. Ensure individually assigned aspects of the project proceed in compliance with cGMP, regulations, and our Company's Quality Management System. Provide… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the Associate Director (AD) is responsible for structuring facilitating and monitoring external-facing agreements including, but not limited to, Master Service ... budgeting guidance. Collaborating with cross-functional teams to ensure contractual compliance and driving continuous improvement. Works closely with suppliers to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.Summary Assist in planning ... performance against project goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities Prior TMF… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …ensuring best practices in SEO and SEM. The owner conducts industry research , facilitates training sessions, manages SEM campaigns, performs keyword analysis, and ... coordination with agencies for Medical/Regulatory/Legal review planning schedules Best Practice Research and Documentation: Conducting research on industry best… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Job Summary: The ... oversight, performance, and management of CRO(s) and 3rd party vendors to ensure compliance with Daiichi Sankyo's quality measures and adherence to scope of work… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.Responsibilities Acts as legal ... media relations, internal communications, public disclosures, social media policies, compliance , crisis communications, and diversity initiatives. Develops contract templates,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating ... a distinct R&D community based on collaboration, partnerships, and cutting-edge research across multiple innovative modalities and therapeutic areas. Our East Coast… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …alignment with broader business objectives. Additionally, the role involves monitoring and analyzing portal performance metrics to drive continuous improvement ... by overseeing UX design efforts. This includes conducting user research , usability testing, and user interface (UI) design to...ensure alignment to broader UX / UI strategy Performance Monitoring and Analysis: Monitoring and analyzing portal… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. SUMMARYProvide support to ... that the organization is in a perpetual state of compliance as follows:Support the Global Quality Lead(s) (GQLs) and...Oncology and Specialty Medicine strategic priorities, by reviewing and monitoring the status of Quality Events (QEs), CAPAs and… more
- Merck & Co. (Rahway, NJ)
- …on all power generation equipment and processes.Lead power generation compliance program including continuous emissions monitoring .Supports capital project ... support the Rahway Campus as well as our Company's North America research facilities including Rahway, Boston, Cambridge, South San Francisco to execute utility,… more
- Merck & Co. (Durham, NC)
- …Assurance (SFQA) B160 to support process and technology introduction, compliance improvements, and manufacturing readiness to initiate production of commercial ... the project lifecycle.Ensure all aspects of the Shop Floor QA proceed in compliance with cGMP, regulations, and our Company's Quality Management System focusing on… more
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