- Merck & Co. (Austin, TX)
- …into technical automation designStrong understanding of RESTful APIs, data pipelines, and platform integrationsPreferred Qualifications: Experience with UIPath, ... by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site...not apply to roles that have been designated as " remote ".The salary range for this role is $114,700.00 -… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJOB DESCRIPTION SUMMARYThe Associate Principal Scientist is a DVM/VMD and/or PhD whose primary function is to design, coordinate, monitor, and report ... (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies.The Associate Principal Scientist is the primary clinical study team leader and has overall… more
- Merck & Co. (Rahway, NJ)
- …Description Director, Combination Product Regulatory CMC - (R5)- - - This Principal Scientist position is equivalent to a Director position. Under direction from the ... Combination Product Regulatory CMC Team Leader, the Principal Scientist is responsible for executing in the Regulatory CMC space. - Leveraging demonstrated… 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
- Merck & Co. (North Wales, PA)
- …SummaryUnder the guidance of a senior leader, a Principal Scientist /Director, has primary responsibility for developing value evidence strategies, and ... authors study protocols, develops measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director (Principal Scientist ) has primary responsibility for the planning and directing of clinical research activities involving new or marketed ... clinical study protocols to overseeing protocol adherence to assessing patient-level data , ensuring data completeness and integrity, and ultimately interpreting… more
- Merck & Co. (Rahway, NJ)
- …Health is seeking a motivated individual to work as a bioanalytical bench scientist within its Good Laboratory Practices (GLP) bioanalytical laboratory. This is a ... bioanalytical scientist position with primary duties in preparing and analyzing...setting up instrument analysis, and processing and interpreting LC-MS/MS data .Assurance that notebooks and other documentations are up to… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJob Description The Senior Scientist , Device Design Control Lead, is a crucial member of our team, responsible for spearheading design control efforts ... through launch and post-market surveillance. Key Responsibilities and Activities: The Senior Scientist , Device System - Device Design Control will be responsible for… more
- Merck & Co. (Rahway, NJ)
- …products to produce safe, effective, innovative medicine. -The Early Clinical Scientist /ECS coordinates the design, planning and execution of early phase clinical ... -Ensures excellence in execution/compliance to support study objectives and data validity. Manages internal/external team performance to achieve project objectives… more
- Merck & Co. (Rahway, NJ)
- …Enabling Technologies Department in Rahway, New Jersey is seeking a Senior Scientist to expand our capabilities to design and engineer proteins with novel ... days may vary by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site presence.This Hybrid work… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Director (Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new or marketed ... days may vary by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site presence.This Hybrid work… more
- Merck & Co. (South San Francisco, CA)
- …Laboratories in South San Francisco is seeking a lab based Senior Scientist with experience in biochemical/biophysical assays and lead discovery support to join ... screening and mechanistic studies using diverse experimental methodologiesEnsure high-quality data generation, analysis, and timely report to project teamsLeverage… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are seeking a highly motivated Senior Principal Scientist to join our collaborative Biophysics group within the Mass Spectrometry & Biophysics ... scientists to drive our core mission. Key Responsibilities: The Senior Principal Scientist , Biophysics will be accountable for:Overseeing a portfolio of projects in… more
- Merck & Co. (Rahway, NJ)
- …to produce safe, effective, innovative medicine.The Senior Principal Scientist /Senior Director is responsible for protocol development and medical/scientific ... days may vary by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site presence.This Hybrid work… more
- Merck & Co. (Rahway, NJ)
- …Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new ... days may vary by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site presence.This Hybrid work… more
- Merck & Co. (North Wales, PA)
- …programming analyst will gather and interpret user requirements, retrieve the required data , transform the data into modeling-ready analysis datasets, and ... analysis plans.-- The programming analyst will take on a data stewardship leadership role and be accountable for the...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (North Wales, PA)
- …and global human health.Responsibilities: The Senior Statistical Programmer, Submission Data Standards Quality Management (SDS QM), provides oversight and quality ... management of submission data standard deliverables for world-wide regulatory application submissions of...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (Rahway, NJ)
- …author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and ... (AMCP) dossiers for US payers, and Global Value Dossiers.Develop supplementary clinical data package in close partnership with markets and HTA statistics group 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 document ... study reports, and new drug application filing. Produce SAS data transport files and program text files for regulatory...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (Rahway, NJ)
- …in developing analysis and reporting deliverables for R&D projects ( data ,-analyses, tables, graphics, listings)- A project leader; completes tasks independently ... Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO,-SAS/GRAPH; systems and database expertise- Designs and… more
