| Resume alert | Resumes 1 - 10 of 574 |
Clinical Research Business Development
Plainsboro, NJ
... sales and marketing and opinion leaders to develop and implement products labelling strategy to meet the requirements of the FDA and other regulatory agencies to achieve enhanced FDA’s agreements to company’s approval desires based on products ... - Apr 21
... sales and marketing and opinion leaders to develop and implement products labelling strategy to meet the requirements of the FDA and other regulatory agencies to achieve enhanced FDA’s agreements to company’s approval desires based on products ... - Apr 21
Senior Manager / Associate Director
Lawrence Township, NJ
... Maintained rigorous compliance in clinical trial operations, meticulously ensuring that all patient-related content aligned with FDA regulations and Bristol-Myers Squibb (BMS) guidelines. As well as ensuring that all CMC practices were updated ... - Apr 18
... Maintained rigorous compliance in clinical trial operations, meticulously ensuring that all patient-related content aligned with FDA regulations and Bristol-Myers Squibb (BMS) guidelines. As well as ensuring that all CMC practices were updated ... - Apr 18
Medical Assistant Pharmacy Technician
Lawrenceville, NJ
... Skills Used Documentation Skills, Analyzing Information, Chemistry Techniques, Informing Others, FDA Health Regulations, Creating a Safe, Effective Environment, Infection Control, Training Management, Lab Environment, Clinical Lab Testing, ... - Apr 13
... Skills Used Documentation Skills, Analyzing Information, Chemistry Techniques, Informing Others, FDA Health Regulations, Creating a Safe, Effective Environment, Infection Control, Training Management, Lab Environment, Clinical Lab Testing, ... - Apr 13
Case Management Customer Service
Plainsboro, NJ
... Implemented new processes that maintain a highly FDA regulated site and a network security design to ensure adherence of HIPPA regulations. Redesigned computer network. Effectively executed new network policies and procedures. Responsible for ... - Apr 04
... Implemented new processes that maintain a highly FDA regulated site and a network security design to ensure adherence of HIPPA regulations. Redesigned computer network. Effectively executed new network policies and procedures. Responsible for ... - Apr 04
Formulation/scale up of solid dosage forms
East Brunswick, NJ, 08816
... Supported technology transfer related activities from development to launch for drug products (DPs) at BMS manufacturing sites (or external manufacturing) according to BMS directives, ICH, FDA and regulatory guidelines. Performed physical testing on ... - Apr 03
... Supported technology transfer related activities from development to launch for drug products (DPs) at BMS manufacturing sites (or external manufacturing) according to BMS directives, ICH, FDA and regulatory guidelines. Performed physical testing on ... - Apr 03
Drug Safety Information Technology
Belle Mead, NJ
... • Expert knowledge of Global and FDA Regulations supporting the submission of Adverse Events for Post- marketing and Clinical Trials drugs. • Understanding of ICH guidelines on PV and application of guidelines detailed in FDA 21 CFR Part 11, ... - Mar 29
... • Expert knowledge of Global and FDA Regulations supporting the submission of Adverse Events for Post- marketing and Clinical Trials drugs. • Understanding of ICH guidelines on PV and application of guidelines detailed in FDA 21 CFR Part 11, ... - Mar 29
Quality Assurance Project Management
North Brunswick, NJ
... Document Management System), SAP(System Applications products in Data Processing) - Provide all necessary documents to FDA, visitors and auditors by putting uncontrolled copies stamp - To maintain all inventories required for documentation. ... - Mar 17
... Document Management System), SAP(System Applications products in Data Processing) - Provide all necessary documents to FDA, visitors and auditors by putting uncontrolled copies stamp - To maintain all inventories required for documentation. ... - Mar 17
United States Materials Handler
Raritan, NJ
... sap knowledge October 2021-February 2022 Materials Handler Ortho-Clinical Diagnostics Raritan, New Jersey, United States Safely and accurately process Customer products according to established procedures within FDA, ISO, and GMP guidelines. ship ... - Mar 01
... sap knowledge October 2021-February 2022 Materials Handler Ortho-Clinical Diagnostics Raritan, New Jersey, United States Safely and accurately process Customer products according to established procedures within FDA, ISO, and GMP guidelines. ship ... - Mar 01
Project Management Business Analyst
East Brunswick, NJ
... • Conducted assays and test methods according to 21 CFR and FDA guidelines, including ELISA, BCA (colorimetric assay), LAL endotoxin, SDS-PAGE, and cell culture technique TLR-5 assay (in training). BRISTOL MYERS SQUIBB, Plainsboro, NJ 2004 - 2009 ... - Feb 28
... • Conducted assays and test methods according to 21 CFR and FDA guidelines, including ELISA, BCA (colorimetric assay), LAL endotoxin, SDS-PAGE, and cell culture technique TLR-5 assay (in training). BRISTOL MYERS SQUIBB, Plainsboro, NJ 2004 - 2009 ... - Feb 28
Analytical, great communicator, strategic, planning & organized
Pennsauken, NJ
... lung, and gastric cancers across 15 sites in the United States from start-up activities including feasibility, final protocol, FDA follow-up, study and site contracts and budgets, master ICF development and approval, oversight of site ICF ... - Feb 18
... lung, and gastric cancers across 15 sites in the United States from start-up activities including feasibility, final protocol, FDA follow-up, study and site contracts and budgets, master ICF development and approval, oversight of site ICF ... - Feb 18