- Merck & Co. (Rahway, NJ)
- …(GCP) studies, and occasionally Good Laboratory Practice (GLP) studies.The Associate Principal Scientist is the primary clinical study team leader and has ... Job DescriptionJOB DESCRIPTION SUMMARYThe Associate Principal Scientist is a DVM/VMD and/or PhD whose primary...Respect - Inclusion.Design and organization of paper and Electronic Data Capture (EDC) clinical studies that meet… more
- Merck & Co. (Rahway, NJ)
- …Testing, Clinical Trial Planning, Clinical Trials Logistics, Clinical Trials Monitoring, Consultative Approach, Cross-Cultural Awareness, Data Analysis, ... Job DescriptionOur Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and… more
- Merck & Co. (Rahway, NJ)
- … Sciences, Clinical Testing, Clinical Trial Planning, Clinical Trial Support, Cross-Functional Teamwork, Data Analysis, Hematology, Intellectual ... Job DescriptionThe Director (Principal Scientist ) has primary responsibility for the planning and...has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines.… more
- Merck & Co. (Lower Gwynedd, PA)
- …contribute to optimization and troubleshooting of assays, method validation, and testing clinical samples.The responsibilities of the Scientist will be to work ... immunology and analytical biochemistry to impact bioanalytical procedures supporting clinical studies.Responsibilities:Generation of quality experimental data to… more
- Merck & Co. (Rahway, NJ)
- …testing using tensile tester or other laboratory equipment and analyze data to inform process development activities.Assist clinical manufacturing team ... & Development team that designs and develops benchtop/low-volume to high-volume clinical and commercial assembly equipment and processes for medical devices/drug… more
- Merck & Co. (North Wales, PA)
- …Care Pharmacy (AMCP) dossiers for US payers and Global Value Dossiers.Develops supplementary clinical data package in close partnership with markets and HTA ... 10%Flexible Work Arrangements:Not ApplicableShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aRequired Skills:Biostatistics, Clinical Development, Communication, Data Management, Epidemiology, Health… more
- Merck & Co. (Upper Gwynedd, PA)
- …Clinical Medicine, Clinical Neurophysiology, Clinical Research Management, Clinical Testing, Clinical Trial Development, Data Analysis, Decision ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide...teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs,… more
- Merck & Co. (Rahway, NJ)
- …to join Biologics Process Research & Development (BPR&D) as a Principal Scientist .BPR&D within Research Laboratories is on a mission to rapidly deliver diverse ... To achieve this, we work closely with colleagues in Discovery, Pre- clinical , Early Development, Analytical, Formulation, and Commercial Manufacturing while providing… more
- Merck & Co. (North Wales, PA)
- …Clinical Study Design, Clinical Testing, Clinical Trial Management Processes, Clinical Trials Analysis, Data Analysis, Data Management, Data ... Job Description Position Description This position is for a principal scientist in biostatistics.-The candidate should have a solid knowledge of statistical… more
- Insmed Incorporated (San Diego, CA)
- …ranging from purification development and optimization, process characterization and clinical manufacturing investigation support. As part of this collaborative ... to keep you challenged and engaged. If you are a driven and astute scientist who is motivated to bring life-changing medicine to patients, then this is the… more
- Merck & Co. (Rahway, NJ)
- …drug/vaccine projects under supervision in Late Development Statistics. --Interacts with Clinical , Regulatory, Statistical Programming, Data Management and other ... and ascertains needs for potential program development of novel statistical methodology.Analyzes data and interprets results from clinical trials to meet… more
- Merck & Co. (Rahway, NJ)
- Job Description BPR&D Downstream Principal Scientist Job Description: - - Our Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, ... bioprocessing to join Biologics Process Research & Development (BPR&D) as a Principal Scientist .- - BPR&D within our company's Research Lab oratories is on a mission… more
- BioAgilytix (Durham, NC)
- …need them.Our Liquid Chromatography/Mass Spectrometry (LC/MS) team is seeking a Scientist III to serve as Bioanalytical Project Manager (BPM)/Principal Investigator ... we tackle challenges across the spectrum of drug discovery to clinical diagnostics, driving advancements that shape the future of healthcare.Essential… more
- Merck & Co. (North Wales, PA)
- …and information into simple readable formSolid project management skillsFamiliarity with clinical data management conceptsStrategic thinking - ability to turn ... 10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):N/ARequired Skills:Business, Business, Clinical Data , Clinical Databases, … more
- Merck & Co. (Rahway, NJ)
- …on our discovery organization, from target identification through delivery of clinical candidates across our fast-growing peptide project portfolio. With in-house ... drug discoverySkilled in scientific programming (eg Python, Pipeline Pilot) and data analytics (eg Spotfire) and democratizing coding and workflowsPassion for… more
- Merck & Co. (Rahway, NJ)
- …and biostatisticians and/or epidemiologists within BARDS, as well as stakeholders in data management, medical writing, and clinical operations to gather and ... following CDISC standards. Generate tables, listings, and graphics required for clinical trial decision-making, regulatory requests, clinical study reports, and… more
- Merck & Co. (Rahway, NJ)
- …document user requirements for statistical programming deliverables.Programmatically synthesize preclinical data into analysis ready structures from varied data ... validate and maintain modeling-ready datasets by integrating PK, PD and covariate data .Produce tables and graphics for inclusion in study reports and regulatory… more
- Merck & Co. (Rahway, NJ)
- …be programmed, an understanding of statistical terminology and concepts.Familiarity with clinical data management conceptsExperience in CDISC and ADaM ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Merck & Co. (North Wales, PA)
- …and programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data , transform the ... ADaM standards is also required.Must possess significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH… more
- Ochsner Health (New Orleans, LA)
- …standard protocols and procedures; performs laboratory tests and calculations to provide data for use in diagnosis and treatment of disease; performs quality control ... Required - Bachelor's Degree in medical technology, medical laboratory science, clinical laboratory science, or chemical, physical or biological science. Copy of… more
