- Eisai, Inc (Nutley, NJ)
- …responsibilities.Ensures the timely and appropriate collection, organization, and analysis of diverse data sources (eg, clinical trial data , patient ... The incumbent will assume a crucial role within the Global Value & Access (GV&A) team, responsible for leading...statistical methodologies and their application in the context of non- clinical studies and related projects in AD and other… more
- Eisai, Inc (Nutley, NJ)
- …strengthen compliance with GDPR, HIPAA, CSL, and other relevant security and data privacy standards . Your responsibilities span security operations, risk ... optimization. Essential Functions: Partnerships and Business Relationships:Promotes awareness of standards related to security, regulatory, clinical , commercial,… more
- Eisai, Inc (Nutley, NJ)
- …reports, cumulative reports, or international regulatory reports and requests. 20%Set standards for data collection and distribution processes; coordinates with ... meet respective goals and regulatory responsibilities. 20% Requirements Application of clinical medicine to patient careMedical terminology and standards of… more
- Merck & Co. (Rahway, NJ)
- …in a timely manner and in coordination with the studyCRM and CRA.Interface with GCTO( Global Clinical Trial Operations) partners on clinical trial execution ... quality standards internally and externally.Under the oversight of the CRD( Clinical Research Director) / Director, Clinical Research, the individual is… more
- Merck & Co. (Rahway, NJ)
- …forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Development Sciences and Clinical Supply (DSCS) enables Drug ... Job DescriptionOur Company is a global health care leader with a diversified portfolio...Substance, Drug Product, Analytical Development, and Clinical Supply across all modalities. We are interdependent across… more
- Merck & Co. (Rahway, NJ)
- …systems and database expertise. Familiarity with statistical analysis methods and clinical data management concepts.US and/or worldwide drug or vaccine ... of deliverable quality and process compliance, (2) effective deliverable development utilizing global and TA standards that optimize analysis and reporting and… more
- Merck & Co. (Rahway, NJ)
- … trial programming, systems and databases including advanced knowledge of CDISC data standards ; experience leading the activities of a programming team ... drug and vaccine programs.Interact with cross functional scientists including, Statistics, Clinical , Regulatory, QP2, CSRM, Data Management and Statistical… more
- Insmed Incorporated (Manhattan, NY)
- Company DescriptionInsmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most ... mission to transform the lives of patients. They must possess a high clinical aptitude and experience in portfolio selling environment to engage key customers. Along… more
- Merck & Co. (Rahway, NJ)
- …area capabilities. Partnering with key stakeholders, individual will benchmark competitor clinical data , business models and capabilities to develop insights ... and recommendations that will help enhance global and regional strategy. The individual will proactively facilitate the identification and prioritization of… more
- Merck & Co. (Rahway, NJ)
- …direction to divisional stakeholders on an improved Digital Technology Strategy, with data analytics at the forefront. -Partner with our Company's research division ... technology execution inclusive of Scope, Quality, Timeline and Budget.Set clear performance standards and key results and hold self and team members accountable for… more
- Merck & Co. (Rahway, NJ)
- …performing manufacturing, packaging, labeling, analytical testing, and distribution supporting the clinical supply chain on behalf of our company. Key activities ... of issues affecting quality and efficiency. -Reviews draft policy and standards .Communicates with senior management within our company and the third-party… more
- Merck & Co. (Rahway, NJ)
- …development of new assay platforms, benchmarking current approaches/techniques to industry standards , and providing technical leadership of design of experiments and ... data interpretation.-Applicants must have effective organizational, multi-tasking, oral/written communications...of release, characterization, and stability assays for testing of clinical trial material and in support of product and… more
- Merck & Co. (Rahway, NJ)
- …activities throughout the facility.-Primary Responsibilities:Provide process support for clinical manufacturing and R&D processes while also facilitating tech ... work to design, install, and qualify new equipment to support GMP clinical production. -Execute and develop appropriate system validation, change control, and… more
- Kedrion Biopharma, Inc. (Fort Lee, NJ)
- …in hematology, immunology, neurology, and transfusion medicine. The **Vice President of Global Clinical Development and Strategy** will report into an Executive ... individual clinical trials + Collaborate with Kedrion Global Clinical Research teams to drive scientific...+ Maintain current knowledge of strategic trial design and data generation to include registries and real-world data… more
- Rockefeller University (New York, NY)
- …regarding the clinical research study + Collect and process research data and specimens as needed/required + Provide assessment skills and direct nursing care ... of both the virus and our antibodies. Overview The Clinical Research Nurse will be responsible for coordinating and...through the development or updating of protocols, procedures, and standards for a study in collaboration with the primary… more
- Actalent (Parsippany Troy Hills, NJ)
- …of their drug candidates are invented and developed in house! Description: + Clinical Data Manager who will work collaboratively with vendor Project Managers ... and Clinical Data Managers to assure that ...according to company SOPs and in compliance with Company's data standards . + Serve as primary DM… more
- Merck (Rahway, NJ)
- …heavily relies on accurate data collected from patients who are part of Clinical Trials. Trial Standards , Trial Design, Trial Data Collections, Trial ... trial participants, in the right way to enable the Clinical Research to analyze data for efficacy,...first site ready. + Remove obstacles and enable the Global Clinical Trial Organization to focus on… more
- Abbott (Manhattan, NY)
- …other clinical site management colleagues and supports key projects/initiatives in Global Clinical Operations and/or Business Units. **What You'll Work On** ... Monitors to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards inclusive of...sites for accuracy and completeness + Facilitate resolution of data queries and action items at clinical … more
- Edwards Lifesciences (Newark, NJ)
- …. **How you will make an impact:** + Design, create, validate, and modify clinical databases, and tools and programs for data validation checks, and ... in the design and delivery of moderately complex functional modules and provide data management expertise regarding clinical trials, protocols, and case report… more
- STERIS (New York, NY)
- Clinical Perioperative Liaison Req ID: 43006 Job Category: Service/Technical Services New York City, NY, US, 10021 Description: At STERIS, we help our Customers ... responsibility of the Perioperative Support Liaison is to provide integrated clinical and technical on-site Customer support, consultation, and management of medical… more
