- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist , Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management ... through launch and post-market surveillance. Key Responsibilities and Activities: The Associate Principal Scientist , Device System - Device Risk Management will… more
- Merck & Co. (MA)
- 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
- Merck & Co. (Rahway, NJ)
- 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. (Rahway, NJ)
- 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** The Associate Principal Scientist , Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management ... launch and post-market surveillance. **Key Responsibilities and Activities:** The Associate Principal Scientist , Device System - Device Risk Management will… more
- J&J Family of Companies (Spring House, PA)
- …Johnson & Johnson Innovative Medicine R&D is recruiting for a Senior Principal Scientist , Nonclinical Safety Lead within Preclinical Sciences and Translational ... a hybrid role and will be located in Spring House, PA. As a Senior Principal Scientist , Nonclinical Safety (NCS) Lead, you will collaborate with innovative and… 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 (Rahway, NJ)
- **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
- 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
- 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
- J&J Family of Companies (Spring House, PA)
- …& Johnson Innovative Medicine R&D is recruiting for a Distinguished Scientist , Nonclinical Safety Leader within Preclinical Sciences and Translational Safety (PSTS). ... role and will be located in Spring House, PA. As a Distinguished Scientist , Nonclinical Safety (NCS) Leader, you will collaborate with innovative and diverse… 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
- Conagra Brands (Chicago, IL)
- Reporting to the Director of R&D, you will lead research and development projects and technology initiatives within the growing meat snacks category. You will serve ... industry standards of quality and food safety, FDA regulations, and government regulatory requirements in food processing + Demonstrated exceptional competence in a… more
- UTMB Health (Galveston, TX)
- …utilize the US FDA GLP regulations as a reference standard. The Regulatory Scientist II may also function as a Principal Investigator for extramurally funded ... Select Agent Program (FSAP). **JOB SUMMARY** **Function** : The Regulatory Scientist II will be assigned as...Scientist II will be assigned as a Study Director , as defined by the US FDA Good Laboratory… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …of the responsible Emory faculty director , the Assistant Academic Research Scientist may serve as the principal investigator on funded (grant) proposals. ... to the excellence of our academic community. **Description** The Scientist will play a key role in advancing basic...trainees. + Contribute to the preparation and submission of regulatory documents such as IACUC, IRB, and Biosafety applications.… more
- Merck (Boston, MA)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …Lead, Clinical Scientist . and other functional areas such as GCO, biostats, regulatory , pharmacovigilance. The Director will be a key contributor to INDs, ... NDAs, BLAs, and other global regulatory filings and publications. The Director will...in the academic environment and/or acted as an assistant Principal Investigator or Principal Investigator. + May… more
- Fenway Health (Boston, MA)
- …approval and assistance of the site Principal Investigator or research scientist , ensuring adherence to ethical and regulatory standards. + Meeting ... Communication:Regularly communicate initiatives, progress, and updates to the Project Director and Principal Investigator, ensuring transparency and alignment… more
- Mayo Clinic (Scottsdale, AZ)
- …the training in advanced career skills such as grant writing for NIH and regulatory work with the Food and Drug Administration (FDA). Future career goals for the ... 33437588; Nature BME PMID: 31015715). Dr. Oklu is a physician- scientist with a Ph.D. in biochemistry and is a...Vascular and Interventional Radiology at Mayo Clinic and the Director of the Laboratory for Patient Inspired Engineering. Dr.… more
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