- Merck & Co. (Rahway, NJ)
- Job DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead (Associate Director Equivalent) Our company's Device Product & Process ... products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional… more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... the clinical instruction(s) and commercial market approval(s) of combination products. Principal ResponsibilitiesLead, set direction, align with key stakeholders, and… more
- Merck & Co. (North Wales, PA)
- …state-of-the-art technology and applying rigorous scientific and ethical standards.The Senior Director (Senior Principal Scientist ) has primary ... to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new...post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development,… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionThe Clinical Director ( Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research activities ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Clinical Director May Be… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research activities ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director May Be… more
- Organon & Co. (Jersey City, NJ)
- …Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the Associate Principal Scientist is responsible for developing and implementing ... Description** **The Position** Reporting to the Director or Executive Director in...global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and… more
- Organon & Co. (Plymouth Meeting, PA)
- …Description** **The Position?** Reporting to the Director in Organon Regulatory CMC,?the Associate Principal Scientist is responsible for?developing ... in accordance with global regulations and?guidance, and?Organon procedures.? The Associate Principal Scientist will lead the?preparation and submission of CMC… more
- Arvinas (New Haven, CT)
- …more information, please visit www.arvinas.com . **Position Summary** The Clinical Scientist is responsible for providing scientific support for all Global Clinical ... medical experts both internal and external to the company. The Clinical Scientist needs to possess the ability to think creatively, function independently, deliver… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director … more
- Merck (West Point, PA)
- **Job Description** **Associate Principal Scientist - Device Technical and Engineering Lead (Associate Director Equivalent)** _Our company's Device Product & ... ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead… more
- Merck (Rahway, NJ)
- …and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will lead the definition and execution of ... clinical instruction(s) and commercial market approval(s) of combination products. ** Principal Responsibilities** + Lead, set direction, align with key stakeholders,… more
- Catalent Pharma Solutions (Baltimore, MD)
- …on Quality by Design principles and regulatory compliance. The Principal Scientist will report to the Senior Director of Analytical Development and is ... ** Principal Scientist , Analytical Development** **Summary:** Catalent...Scientist - Analytical Development will report to the Senior Director , Analytical Development. **Catalent is committed to a Patient… more
- Merck (North Wales, PA)
- …technology and applying rigorous scientific and ethical standards. The Senior Director (Senior Principal Scientist ) has primary responsibility ... to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new...post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development,… more
- Merck (North Wales, PA)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Director May… more
- Merck (Boston, MA)
- **Job Description** The **Clinical Director ( Principal Scientist )** has primary responsibility for the strategic planning and directing clinical research ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May… more
- J&J Family of Companies (Spring House, PA)
- …at https://www.jnj.com/innovative-medicine **We are searching for the best talent for a Principal Scientist , Toxicology in Spring House, PA.** **Purpose:** This ... Principal Scientist in Nonclinical Safety and Submissions, a department in...relevant experience is required. + Experience as a Study Director or Study Monitor conducting/overseeing in vivo toxicology studies… more
- Amgen (Washington, DC)
- …us and transform the lives of patients while transforming your career. **Senior Principal Scientist - Global Diagnostic Development Lead** **What you will do** ... assay to marketed Diagnostic to support the clinical development strategy for regulatory approval and commercialization. As such, the Dx group works closely with… more
- UTMB Health (Galveston, TX)
- Regulatory Scientist I / II - Institutional Office... Scientist II will be assigned as a Study Director , as defined by the US FDA Good Laboratory Practice ... for the interpretation, documentation and reporting of results. The Regulatory Scientist I / II works in...I / II works in conjunction with the Scientific Director for the Institutional Office of Regulated Nonclinical Studies… more
- AbbVie (Irvine, CA)
- …analytical method transfer/optimization/validation, product characterization, regulatory submission, and continuous improvement for ... join us as a Group Leader based in Irvine, CA reporting to the Director , PDS&T Toxins. Responsibilities + Manage the protein characterization group by working with a… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …Protein Discovery Department, and will report to the New Proteins &Technology Associate Director . We are seeking a highly motivated and experienced individual with a ... a complex nature, assimilating information across functional areas, suitable for regulatory submission or external publication. + Directs resources in the… more
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