- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …an equal opportunity employer including veterans and people with disabilities. Summary The Associate Director, Clinical Data Standards, is responsible for ... - Leadership, Direction, and Strategy:Leads implementation of Therapeutic level clinical data collection requirements including cross-functional standards… more
- Merck & Co. (Rahway, NJ)
- …and innovative solutions that enable new SAP capabilities and technologies. As the Clinical Manufacturing Delivery Lead for our Research & Development Division , you ... will be responsible for delivering SAP solutions to our Global Clinical Manufacturing user community. You will p articipate in interviews with our company's'… more
- Insmed Incorporated (Bridgewater, NJ)
- …Best Workplaces in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Associate Director, Clinical Project & Planning Management is a member ... finalization of materials, and distribution to executive leadership.Manages vendor(s) for clinical trial data visualization dashboards to ensure accuracy of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …centered around rare diseases and immune disorders.SummaryThis position serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple ... surveillance and risk management in partnership with Product Safety Lead(s), Clinical Safety Physician(s), and cross-functional team in support of benefit risk… more
- Novo Nordisk Inc. (WA)
- …a difference? The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific ... relevant regulatory requirements Ensure accuracy, validity and completeness of data collected at clinical trial sites in...validity and completeness of data collected at clinical trial sites in accordance with the protocol, Monitoring… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …are achieved according to agreed quality standards and timelines and that quality of data is suitable for regulatory submission. The Associate Director will have ... trial master file is complete and accurate for assigned stud(ies).If assigned, Associate Director, Clinical Operations may act as the Study Team Leader for the… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …applications and best practices as well as strong technical skills in working with ( clinical ) data . The position holder will require strong skills in continuous ... understanding and translation of business needs to AI/ML tasks, over data understanding and preparation, to modeling, validation and dissemination- Identify… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionIt is critical that, for all company-sponsored clinical trials, patient safety, high quality data and compliance with company requirements and ... along TA and/or functional lines. - -This includes line management of Country Clinical Quality Managers (CCQMs) and Associate Country Clinical Quality… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionBiologics Process R&D Associate ScientistOur Research Scientists are our Inventors.- Using innovative thinking, state-of-the-art facilities, and ... To achieve this, we work closely with colleagues in Discovery, Pre- clinical , Early Development, Analytical, Formulation, and Commercial Manufacturing while providing… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …or More Years Minimum 7 years' experience in life sciences, pharma with Clinical Trials Operational Data , Clinical Operational Metrics and Milestones. ... required4 or More Years Experience in working with CRO data for execution of large global clinical ...CRO data for execution of large global clinical trials. requiredSolid understanding of Metrics, KPIs, KRIs and… more
- Merck & Co. (Rahway, NJ)
- …of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New Jersey research ... facility.- The Associate Principal Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of biology,… more
- Catalent (St. Petersburg, FL)
- QC Associate Scientist IIThe QC Associate Scientist II supports testing and release of raw materials, intermediate and finished products, and all critical ... of Raw Materials, pre-capsulation, Stability and Finished Products. Analyze data , document results, maintain laboratory notebook according to cGMP and… more
- Merck & Co. (North Wales, PA)
- …preferred)Understanding of clinical research methodology, biostatistics, and clinical pharmacologyFamiliarity with methods of data displayProficiency with ... Job DescriptionDescription: The Associate Principal Scientist, Oncology Publications Medical Writing, works with scientists in our company's Research Labs and… more
- Aequor (Thousand Oaks, CA)
- …this role: Supply Chain Raw Material Procurement experience or Planning or Master Data . Must have previous buying experience as this role will have buying ... experience preferably in the biotechnology or pharmaceutical industry OR Associate 's degree and 6 years of Life Science or...(ie GxP, SOX) High attention to detail Understanding of clinical study conduct Ability to operate in a team… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …standards, and coding library management.Manages, reviews and approves medical coding of clinical data ensuring high quality; creates and manages the ... immune disorders. Summary Position manages the end-to-end delivery of medical coding data for assigned projects/studies collaborating with clinical and medical… more
- Merck & Co. (Rahway, NJ)
- …fast-paced job that provides both technical and project management responsibility. The Associate Specialist - Engineering Auto Eng position will report to the ... and non-capital improvement projects, and the automation systems spanning various clinical manufacturing facilities. In this role, you will be responsible for… more
- Catalent (Emeryville, CA)
- Research Associate II, BioconjugationPosition Summary:Catalent Pharma Solutions in Emeryville, CA is seeking a Research Associate II who will be responsible for ... liquid chromatography) analysis of site-specific antibody-drug conjugates (ADCs). The Research Associate II reports to the Group Leader, Bioconjugation. This is a… more
- Merck & Co. (Rahway, NJ)
- …of the MACS EDFE Leader include the following:The EDFE Leader role at the Associate Director level will serve as a technical mentor and process team member ... (small molecule, macrocyclic peptides, bioconjugates) Drug Substance development and GMP clinical manufacturing plant currently planned in Rahway, New Jersey. The … more
- Merck & Co. (North Wales, PA)
- …from clinical trials as well as analyzing oncology biomarker and clinical data .-Coordinate all statistical activities for ongoing clinical ... health. The incumbent is responsible for statistical planning and data analysis of Phase I/II oncology clinical ...and data analysis of Phase I/II oncology clinical trials as well as translational biomarker analyses. This… more
- Aequor (Thousand Oaks, CA)
- …LIMS (laboratory information management system) and a basic understanding of clinical trials understanding, and a strong understanding of MS Excel.This role ... This will include, but not limited to, monitoring incoming data and files from external vendors and resolving ...data and files from external vendors and resolving data and formatting issues related to incoming manifests, files,… more
