- Merck & Co. (Boston, MA)
- …interaction with key scientific leaders.Specifically, the Senior Principal Scientist is responsible for:Planning clinical trials (design, operational plans) ... to ensure timely and equitable access to our medicines.The Senior Principal Scientist has primary responsibility for... Clinical Medicine, Clinical Research Management, Clinical Trial Development, Clinical Trials, Data… more
- Merck & Co. (North Wales, PA)
- …integrating state-of-the-art technology and applying rigorous scientific and ethical standards.The Senior Director ( Senior Principal Scientist ) has primary ... Senior Director will manage the entire cycle of clinical development, including study design, initiation, execution,-monitoring, analysis, regulatory reporting,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Scientist , Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management efforts in ... concept through launch and post-market surveillance. Key Responsibilities and Activities: The Senior Scientist , Device System - Device Risk Management will be… more
- Aequor (Thousand Oaks, CA)
- …Oaks Global Critical Reagents (GCR) Team is looking for an experienced, hands-on scientist to join the GCR - Process Excellence (GCR-PEX) team. This senior ... This engagement requires conformance with site policies, safety, quality, and data -integrity requirements. The successful candidate must model 's mission and the… more
- Merck & Co. (North Wales, PA)
- …project level Position Specific Required Skills and Experience: Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic ... in CDISC SDTM and ADaM standardsSignificant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPHDesigns… more
- Merck & Co. (North Wales, PA)
- …related drug/vaccine projects in Late Development Statistics.Lead the interaction 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. (North Wales, PA)
- …and information into simple readable form.Solid project management skills.Familiarity with clinical data management concepts.Strategic thinking ability to turn ... deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects.Be accountable for submission data standards… more
- Merck & Co. (Rahway, NJ)
- …Scientist position available at its Rahway, New Jersey research facility. The Principal Scientist is a senior scientific role tasked with working closely with ... scientific understanding of Critical Quality Attributes/QbD/DOE principles as well as data analysis and statistics for setting specifications - Ability to design,… more
- Pfizer (Groton, CT)
- … study results Support execution for all FIH programs through proof-of concept Set the clinical data review strategy, ensure quality data and conduct review ... of emerging clinical data and trends; review and query data ;...driving change across all levels of the organization including senior management. Data listing review experience Critical… more
- Merck & Co. (Rahway, NJ)
- …development and design control principles to positively support and influence clinical and commercial combination product development and launches to ensure they ... Regulatory teams to ensure compliance with applicable global regulations. Leverage data analytics and key performance indicators to monitor process performance.… more
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