- Merck & Co. (North Wales, PA)
- …execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on a clinical trial team.Leading medical monitoring ... mentorship to other clinical scientists.Core Skills: Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH)Ability to manage… more
- Merck & Co. (North Wales, PA)
- …commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; andAssist the Senior /Executive Director in ... clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Director May Be Responsible… more
- Merck & Co. (North Wales, PA)
- …commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; andAssist the Senior /Executive Director in ... clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.Evaluating pre- clinical and translational… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDescription:The Senior Principal Scientist reports to the Senior Director Chemical Biotechnologies of Process Research & Development Enabling ... of others, and in driving the scientific strategy of the CBT group. The Senior Principal Scientist manages and prioritizes a portfolio of work that includes… more
- Merck & Co. (Rahway, NJ)
- …people from diverse background and expertise, including research scientists, clinical scientists, regulatory experts, IT specialists, etc.Identify opportunities ... responses to data and analysis related queries from research scientists, clinical scientists, and regulatory agencies.--Engage in AI/ML and statistical… more
- Merck & Co. (Rahway, NJ)
- …and execute statistical study and report deliverables ranging from individual clinical trials to world-wide regulatory application submissions.Design and ... Job DescriptionResponsibilities:Support statistical programming activities for clinical development projects.This may include leadership of one or more… more
- Merck & Co. (Rahway, NJ)
- …robust and scalable upstream processes for biologics in different stages of clinical development, 2) process characterization and regulatory filings for ... Job DescriptionPosition Description: Principal Scientist , Upstream Bio Process Development BPR&D within our Company's Research Laboratories is on a mission to… more
- Merck & Co. (Rahway, NJ)
- … Scientist position available at our company's research facility. The Principal Scientist is a senior scientific role tasked with working closely with ... and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process development.A… more
- Lundbeck (Bothell, WA)
- …to determine the potency of drug product for early through late-stage clinical development programs. The successful candidate will have a thorough understanding of ... to the position is a thorough understanding of the regulatory and industry standards that are required for potency...for all development programs (from early to late phase clinical development) Author and review SOPs, development reports, and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical ... in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire...analysis, regulatory filing, and publication. Specifically, The Senior Clinical Director May Be Responsible For:… more
- Merck & Co. (North Wales, PA)
- …with talented and dedicated colleagues while developing and expanding your career.The Senior Clinical Director (Sr. Principal Scientist ) has primary ... clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.- Specifically, the Senior Director may… more
- Merck & Co. (Rahway, NJ)
- …the role of- Senior Specialist.--QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to ... for regulatory documents such as Investigational New Drug application, Clinical Study Report, Common Technical Document, and agency- interactions.-You -will also… more
- Amgen (Thousand Oaks, CA)
- …a career you can be proud of. ** Clinical Pharmacology, Modeling & Simulation- Senior Principal Scientist ** **Live** **What you will do** Let's do this. Let's ... change the world. The Senior Principal Scientist at Amgen is responsible for clinical ...exist for selected dose levels. + Leads preparation of clinical pharmacology contributions to regulatory documents including… more
- Philips (Plymouth, MN)
- ** Senior Clinical Development Scientist ** The Senior Clinical Development Scientist for the Image Guided Therapy Peripheral Vascular group will ... life cycle management._ + _Drive execution ensuring quality and timeliness of clinical programs and/or trials to support critical regulatory requirements, be… more
- Amgen (Thousand Oaks, CA)
- … Clinical Pharmacology, Modeling and Simulation department, the Modeling and Simulation Senior Scientist will support Amgen clinical development and ... time for a career you can be proud of. ** Senior Principal Scientist - Clinical ...modeling reports and supply to the summary documents for regulatory submissions. **Win** **What we expect of you** We… more
- Amgen (Thousand Oaks, CA)
- …best work alongside other innovative, driven professionals in this meaningful role. ** Senior Scientist - Clinical Pharmacology, Modeling and Simulation** ... Clinical Pharmacology, Modeling and Simulation department, the Modeling and Simulation Senior Scientist will support Amgen clinical development and… more
- Danaher Corporation (Sunnyvale, CA)
- …Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Clinical Research Scientist ... team and will be hybrid to Sunnyvale, CA. The senior clinical research scientist will...content of clinical study reports and review clinical and analytical sections for regulatory submissions… more
- Abbott (Maple Grove, MN)
- …Clara, CA or Maple Grove, MN currently has an opportunity for an on-site ** Senior ** ** Clinical Scientist /Project Manager Clinical Evaluation** . This ... and exchange of documents between stakeholders (eg, internal personnel such as Regulatory Affairs, R&D Engineering, Clinical Engineering, A&P and Marketing,… more
- United Therapeutics (Durham, NC)
- …duties as required **For this role you will need** Minimum Requirements + For Senior ( Clinical ) Product Development Scientist level: + Bachelor's degree with ... trial design, study implementation, sponsor/site interactions, scientific and clinical methodology, protocol design, project management and regulatory … more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Senior Manager, Hematology, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity ... provide scientific expertise necessary to design and deliver on clinical studies and programs. As a Senior ... research methodology & medical writing skills. Knowledge of clinical development process, regulatory requirements and ICH/GCP… more
