- Merck & Co. (Rahway, NJ)
- …Quality Operations - API, is responsible for independent review and approval of documentation to support Good Manufacturing Practice (GMP) clinical supply API ... manufacture, testing, release, and maintenance in support of our company's clinical supply programs. This person will also independently review and approve … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThis Senior Engineer position will provide engineering support to the Rahway, NJ FLEx (Formulation, Laboratory & Experimentation) center, primarily ... Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply (PSCS)The FLEx sterile facility supports the formulation and filling… more
- Merck & Co. (Rahway, NJ)
- …to join Biologics Process Research & Development (BPR&D) as a Senior Principal Scientist.BPR&D within Research Laboratories is committed to rapidly delivering ... achieve our goals, we work closely with colleagues in Discovery, Pre- clinical , Early Development, Analytical, Formulation, and Commercial Manufacturing, all within a… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAs a Senior Engineer in Device Design and Process Development group, you will be part of our Research & Development team that designs and develops ... benchtop/low-volume to high-volume clinical and commercial assembly equipment and processes for medical devices/drug delivery systems. Reporting to the Director… more
- Merck & Co. (Rahway, NJ)
- …technical responsibility and leadership of internal and external work.The Senior Scientist, Engineering position leverages scientific/technical experience to develop ... and participating in risk assessments, deviation investigations, and Good Documentation Practices (GDPs).- Position Qualifications :Education Minimum Requirement: The… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Merck & Co. (North Wales, PA)
- …Material(s):Required Skills:Business Development, Business Development, Business Management, Clinical Documentation , Clinical Investigations, ... of assets within the pediatric section of the Vaccine Clinical Development TA.May serve as a senior ... Clinical Judgment, Clinical Reporting, Clinical Research, Clinical Trial Documentation ,… more
- Merck & Co. (Rahway, NJ)
- …including analysis/modeling datasets, tables, listings, figures and associated documentation .Ensure programmatic traceability from data source to analysis/modeling ... field plus 3 years SAS programming experience in a clinical trial environment OR a Bachelor's degree in Computer...field plus 5 years SAS programming experience in a clinical trial environment.Minimum requirement:Must have experience in CDISC SDTM… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …ED&AA, IT, Ethics and Compliance, Commercial, Patient Services, CMR ( Clinical , Medical, Regulatory), Finance, and Novo Nordisk global colleagues. Externally, ... IT teams to ensure a strong data and technology foundation Engage senior leaders to drive strategic technology transformations Physical Requirements 10-20% overnight… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Operations, including but not limited to - Commercial, Patient Services, CMR ( Clinical , Medical, Regulatory), Finance, and Novo Nordisk global colleagues, to deliver ... and rotations.Demonstrate analytics' value in solving complex business challenges.Engage senior leaders to drive strategic analytics transformations.Partner with Data… more
- Merck & Co. (Rahway, NJ)
- …at its Rahway, New Jersey research facility. The Principal Scientist is a senior scientific role tasked with working closely with the group Director to define ... for successful transfer of assays. Plan assay optimization and documentation to meet program deadlines.Authoring and reviewing internal technical reports,… more
- Aequor (Thousand Oaks, CA)
- …Project Planning, an activity that is vital to the impact that ATO B20 with a clinical and commercial product mix has to the network. This role will function as a ... communicating verbally, in writing, and through presentations to peers and senior leadership team. Additional Responsibilities include: Engaging with Quality and… more
- Merck & Co. (Rahway, NJ)
- …To achieve this, we work closely with colleagues in Discovery, Pre- clinical , Early Development, Analytical, Formulation, and Commercial Manufacturing while providing ... and scalable upstream processes for biologics in different stages of clinical development, 2) process characterization and regulatory filings for successful… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …methodologies to provide key insights into the biopharmaceutical landscape across clinical , commercial, and enterprise domains. This role involves applying data ... Sales operations, Market Access and Public Affairs, and enterprise function's clinical and business decision-making is supported by timely, accurate and… more
- Merck & Co. (Rahway, NJ)
- …listings, figures and submission deliverables under the guidance of a senior level programmer.Perform validation tasks according to departmental SOPs and collaborate ... reports and regulatory submissions.Produce SAS transport files and associated documentation for regulatory submissions.Assure deliverable quality and compliance with… more
- Geisinger (Danville, PA)
- Job Summary The Clinical Documentation Improvement Program is designed to improve the physician's documentation in the patient's medical record supporting ... + Provides on-going education to physicians and essential healthcare providers regarding clinical documentation improvement and the need for accurate and… more
- Geisinger (Danville, PA)
- Job Summary The Clinical Documentation Improvement Program (CDI) is designed to improve the physician's documentation in the patient's medical record, ... of care of the patient. The role of the Clinical Documentation Improvement Specialist (CDIS) is to...dental and domestic partners. Perhaps just as important, from senior management on down, we encourage an atmosphere of… more
- Sanford Health (Bemidji, MN)
- …& Dynamic Team: Work alongside a knowledgeable, supportive, and forward-thinking clinical documentation team that values collaboration and continuous ... focus on improving patient outcomes through accurate and complete clinical documentation . Career Development Opportunities: Access professional development… more
- Penn Medicine (Philadelphia, PA)
- …applicable guidelines, policies and procedures of IS and UPHS to ensure necessary controls, documentation and audit trails Senior Clinical Analyst: A ... assist with basic hardware configurations, database management tools and query language - preferred Senior Clinical Analyst: A Senior Clinical Analyst… more
- Penn Medicine (Philadelphia, PA)
- …each day. Are you living your life's work? ** Clinical Systems Analyst ( Senior , Mid, Associate)** ** Senior Clinical Systems Analyst-** Job Summary: + ... Systems that integrate with Epic System applications at Penn Medicine. The Senior Clinical Systems Analyst is responsible for analyzing, implementing,… more
