- Merck & Co. (Rahway, NJ)
- …DescriptionJOB DESCRIPTION SUMMARY Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary ... Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader… 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 ... Company and with external partners.Author and review relevant portions of the regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for combination product programs… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position?** Reporting to the Director in Organon Regulatory CMC,?the Associate Principal Scientist is responsible for?developing ... products in accordance with global regulations and?guidance, and?Organon procedures.? The Associate Principal Scientist will lead the?preparation and submission… more
- Organon & Co. (Jersey City, NJ)
- …Director in Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the Associate Principal Scientist is responsible for developing and implementing ... in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Associate Director, Clinical Research Scientist will support and work predominately with ... This individual will provide scientific support to clinical development and operations, regulatory and quality assurance teams, as well as overall program support… more
- Merck & Co. (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions.-We are seeking a strategic and technical leader with ... Provide technical oversight of cell culture process development, process characterization and regulatory filing activities to ensure a smooth and clear path to… more
- Merck & Co. (Rahway, NJ)
- …state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The incumbent is responsible for… more
- Merck & Co. (North Wales, PA)
- …span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.-Design and maintain statistical ... and systems and database expertise;US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the development… more
- SLR Consulting Limited (Fort Collins, CO)
- SLR International Corporation is seeking an Air Quality Associate Consultant to join our Air Quality team. The qualified candidate will have 10 or more years of ... of experience incorporating engineers, geologists, toxicologists, hydrogeologists, remediation specialists, regulatory and compliance specialists, and environmental scientists. We work… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new or ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be… more
- Tidelands Health (Murrells Inlet, SC)
- …Qualifications** + High School Diploma or equivalent Required or + Associate 's Degree in Medical Lab Technology Required **Experience Qualifications** ... Laboratory Technician - American Society for Clinical Pathology Required or + Medical Laboratory Scientist - American Society for Clinical Pathology Required or… more
- Insmed Incorporated (NJ)
- …of project timelines and deliverables. Key trial management support to the Associate Directors (CST Leads), as assigned.What You'll Do: Leads and coordinates the ... all clinical trial activities in compliance with GCP and relevant regulatory guidelines.Detailed management and oversight of regional trial activities, as… more
- Merck (Rahway, NJ)
- …**JOB DESCRIPTION SUMMARY** _Primary activities include but are not limited to:_ The Associate Principal Scientist is a DVM and/or PhD whose primary function ... Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader… more
- IQVIA (Indianapolis, IN)
- We are seeking a **Senior Scientist /** ** Associate Principal Scientist , Ligand Binding Assays** to join IQVIA Laboratories in **Indianapolis, IN** . We hire ... us as we transform and accelerate research and development. As a Senior Scientist / Associate Principal Scientist , you will provide technical leadership across… more
- PNC (Pittsburgh, PA)
- …valued and have an opportunity to contribute to the company's success. As an Associate Data Scientist within PNC's Balance Sheet Analytics & Modeling Marketing & ... drive customer engagement and business growth. We are seeking a skilled and passionate Associate Data Scientist to join our team and build the data… more
- System One (Basking Ridge, NJ)
- Job Title : Associate Director, Clinical Safety Scientist (Contingent Worker) Job Schedule: Candidate can work 100% remote - preference would be EST/CST based ... global electronic signal tracking tool + Collaborates with the PSL(s) and scientist lead to plan and prioritize activities for Biologics License Applications… more
- University of Colorado (Aurora, CO)
- **Open Rank - Assistant, Associate , Professor. Lead Scientist in Psychiatric Neuromodulation Research.** **Description** **University of Colorado Anschutz** ... value-added recruitment advertising agency (https://www.jobelephant.com/) Open Rank - Assistant, Associate , Professor. Lead Scientist in Psychiatric Neuromodulation… more
- University of Miami (Miami, FL)
- …in ensuring the lab adheres to regulatory policies. CORE JOB SUMMARYThe Associate Scientist , SOM supports the University's research goals and objectives by ... Center has an exciting opportunity for a Full Time Associate Scientist to work at the UHealth...offers competitive salaries and a comprehensive benefits package including medical , dental, tuition remission and more. UHealth-University of Miami… more
- University of Miami (Miami, FL)
- …of Pulmonary, Critical Care, and Sleep Medicine has an exciting opportunity for an Associate Scientist . The Associate Scientist contributes to basic ... animals, ensuring their welfare and compliance with ethical guidelines and regulatory requirements. + Maintain laboratory cleanliness and orderliness, including the… more
- Takeda Pharmaceuticals (Boston, MA)
- …GMSci DP/PKG** **Location: Cambridge, MA** **About the role:** As a Process Scientist ( Associate Director) - Global Manufacturing Science GMSci Drug Product ... and the life cycle management of existing products. You will lead regulatory interactions, including the preparation of Chemistry, Manufacturing, and Controls (CMC)… more
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