- 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. (Upper Gwynedd, PA)
- 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
- Formation Bio (New York, NY)
- …to bring new treatments to patients faster and more efficiently.About the PositionAs a Principal Data Scientist - Medical Imaging at Formation Bio, you will lead ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Merck & Co. (Rahway, NJ)
- …SummaryUnder the guidance of a senior leader, an Associate Principal Scientist /Associate Director, has primary responsibility for planning/managing ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck & Co. (North Wales, PA)
- …resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, ... reimbursement. The incumbent is expected to work cross-functionally with clinical development, medical affairs, biostatistics, market access, commercial and country… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryThe Principal Scientist /Director, Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient- reported outcomes assessments, systematic reviews and… more
- Merck & Co. (Rahway, NJ)
- …upstream bioprocessing to join Biologics Process Research & Development (BPR&D) as a Principal Scientist .BPR&D within Research Laboratories is on a mission to ... actively publish and engage with the scientific community to influence the field.As a Principal Scientist you will have the opportunity to influence the future… more
- Merck & Co. (Rahway, NJ)
- 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. (North Wales, PA)
- Job Description Position Description This position is for a principal scientist in biostatistics.-The candidate should have a solid knowledge of statistical ... management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/ III trials.- The knowledge must be… 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. (Rahway, NJ)
- …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)
- …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
- 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
- Bristol-Myers Squibb Company (Princeton, NJ)
- …facilitates the transition of drug candidates from early to late-stage clinical development, their approval and life cycle management. Early-stage translational ... the development, and maximize the potential, of BMS's therapies post- clinical proof-of-concept, including registrations and life-cycle management. Translational disease… more
- Kymera Therapeutics (Watertown, MA)
- Who we are: Kymera is a clinical -stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical ... contribute: We are seeking an experienced Modeling and Simulation scientist to join the Preclinical Development group at Kymera...QSP) to guide decision-making and help optimize therapeutics for clinical success. This is the ideal role for a… more
- Children's National Hospital (Washington, DC)
- …Core at Children's National Hospital is seeking a highly skilled Bioinformatics Scientist to join our team of bioinformatics engineers and scientists. The role ... Bioinformatics Core with matrixed scope of work and responsibilities across Principal Investigators (PIs). A strong background and expertise analyzing single cell… more
