- Merck & Co. (Rahway, NJ)
- … Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies.The Associate Principal Scientist is the primary clinical study team leader ... Job DescriptionJOB DESCRIPTION SUMMARYThe Associate Principal Scientist is a DVM/VMD and/or...primary function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the… 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 Oncology medicines. Our company Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage… 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 Oncology medicines. Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage… more
- Merck & Co. (Rahway, NJ)
- …and pipeline products to produce safe, effective, innovative medicine.The Senior Principal Scientist /Senior Director is responsible for protocol development and ... Job DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries...boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and… more
- Merck & Co. (South San Francisco, CA)
- Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for ... Therapeutic Area Lead in Translational Medicine.Primary responsibilities for the Senior Principal Scientist include the following:Key member of an early… 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 ... downstream bioprocessing to join Biologics Process Research & Development (BPR&D) as a Principal Scientist .- - BPR&D within our company's Research Lab oratories… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, a Principal Scientist /Director, has primary responsibility for developing value evidence ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck & Co. (Rahway, NJ)
- …drug products.We are seeking a highly motivated candidate for the position of Principal Scientist (R5) focused on developing parenteral drug products across a ... Job DescriptionPrincipal Scientist - Mixed Modalities, Sterile Product DevelopmentThe Mixed Modalities team within Sterile Product Development is responsible for… 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 ... group of scientists to drive our core mission. Key Responsibilities: The Senior Principal Scientist , Biophysics will be accountable for:Overseeing a portfolio of… more
- Merck & Co. (North Wales, PA)
- …other team members when opportunities arise. Primary Activities :Programmatically synthesize clinical / preclinical data into analysis ready structures from varied ... or related field plus 9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences,… more
- Merck & Co. (Rahway, NJ)
- …barriers to reimbursement and market access, and provide input into clinical , regulatory, payer/access, marketing and evidence generation strategies and programs.In ... Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers.Develop supplementary clinical data package in close partnership with markets and HTA statistics… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- …programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into ... at least 7 years SAS programming experience in a clinical trial environment OR a Bachelor's degree in Computer...field plus 9 years SAS programming experience in a clinical trial environment. Required Skills and Experience: Experience in… more
- Merck & Co. (Boston, MA)
- …on our discovery organization, from target identification through delivery of clinical candidates across our fast-growing peptide project portfolio. With in-house ... access to the most innovative screening techniques, and world-class medicinal chemistry, this position offers a wealth of opportunities to impact our discovery pipeline and ultimately save and improve patient lives.- Key responsibilities will include:… 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...plasma and other biological samples to support pharmacokinetic, toxicokinetic, clinical efficacy and/or human food safety studies in a… more
- BioAgilytix (Durham, NC)
- … Scientist III to serve as Bioanalytical Project Manager (BPM)/ Principal Investigator (PI), overseeing all aspects of bioanalytical studies-including project ... we tackle challenges across the spectrum of drug discovery to clinical diagnostics, driving advancements that shape the future of healthcare.Essential… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- BioAgilytix (San Diego, CA)
- …Manager II will lead scientific and operational activities in support of preclinical, clinical , and product release studies for our San Diego lab. This role requires ... team(s) developing and validating bioanalytical assays for support of preclinical, clinical and product release studies.Motivating team by inspiring employees to… more
- BioAgilytix (San Diego, CA)
- …studies in biological matrices using LC-MS/MS, supporting preclinical and clinical development across multiple modalities. The remaining 5% will involve ... results, troubleshoot issues, and ensure timely completion of studies.Serve as Principal Investigator or Study Director for GLP/validation projects, reviewing data,… more
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