- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: The Sr. Director , Clinical Safety MD, will lead the development and implementation of ... a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of...and other relevant sources for the prompt identification of safety signals.Lead internal and external (especially regulatory ,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the Sr. Director , representing the Quality organization at senior levels. The Director plays a pivotal role in regulatory inspections, external audits, and ... a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of...and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of… more
- Merck & Co. (Upper Gwynedd, PA)
- …in the execution of clinical studies. --Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and ... changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in...an Associate Vice President in the Oncology Clinical Research Group . Under the guidance of a supervisor, the Senior… more
- Merck & Co. (Rahway, NJ)
- …of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.- Specifically, the Senior Director ... Scientists in the execution of clinical studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …optimize, and innovate signal detection and management processes across the global safety organization. The incumbent will ensure regulatory compliance, promote ... (eg SOPs) as appropriate.Collaborate with cross-functional teams (eg, Medical Safety , Regulatory Affairs, Epidemiology) to ensure benefit-risk integration… more
- Merck & Co. (Boston, MA)
- …development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director ... Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for...execution of clinical studies. Work closely with a cross-functional group of experts in commercialization, regulatory affairs,… more
- Merck & Co. (Rahway, NJ)
- …Ensure that all activities are conducted with the highest regard for safety , quality, and regulatory compliance, aligning with the company's divisional ... Job DescriptionJob Summary: The Director , Combination Product Commercialization is a key leadership role within the Device Development and Technology Organization.… more
- Genmab (NJ)
- …like a fit? Then we would love to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for ... The lead may also be responsible for supporting various regulatory policy and/or intelligence deliverables. This role will be... Affairs (GRA) and will report to the Sr. Director , Labeling, Policy and Intelligence. The position may be… more
- Merck & Co. (Rahway, NJ)
- …agility and flexibility to meet business needs.As leader of the Process Engineering group , the incumbent will be responsible for the evaluation and implementation of ... key stakeholders.Training skills: Ability to train employees in technical, compliance, safety , and environmental procedures; ability to write SOPs and technical… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... Scientists in the execution of clinical studies.Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and… more
- Merck & Co. (Rahway, NJ)
- …development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director ... Job Description-The Senior Director (Senior Principal Scientist) has primary responsibility for...the execution of clinical studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs,… more
- Merck & Co. (Rahway, NJ)
- …cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director ... Scientists in the execution of clinical studies.Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and… more
- Merck & Co. (Rahway, NJ)
- … regulatory submissions.-Under the general scientific and administrative direction of the Director in Biologics Cell Culture Sciences group and working in ... next generation process development and characterization, process validation, and regulatory submission authoringIn this role, the successful candidate will be… more
- City of Spring Hill Kansas (Spring Hill, KS)
- …inspections. Analyze architectural plans and specifications to ensure they meet safety and regulatory standards. Perform field inspections on industrial, ... Brief Description of Duties: Under the supervision of the Community Development Director , the Building Official is an exempt position under FLSA. This employee… more
- Sanofi Group (Morristown, NJ)
- … Director collaborates closely with cross-functional teams, including Global Regulatory Affairs, Clinical Development, Safety , and Medical Affairs, to ... **Job Title:** Associate Director , Global Regulatory Affairs - Global...products throughout their lifecycle. + Collaborate with clinical, medical, safety , and regulatory colleagues to provide labeling… more
- AbbVie (South San Francisco, CA)
- …to serve a Safety Statistics Group Oncology TA Head in our Safety Statistics team. The Director will have oversight of statisticians in oncology. This ... Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Safety Statistics Group (SSG) at AbbVie is an important strategic… more
- EMCOR Group (Raleigh, NC)
- …financial strength and national presence. Southern Industrial Constructors Inc. is seeking a Corporate Director of Safety to work out of our Raleigh, NC office. ... maintenance services in the Southeast. As part of EMCOR Group , Southern Industrial's ability to serve our customers is...The Corporate Director of Safety is responsible for assisting… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Director , Global Regulatory Labeling Strategy where you will be responsible for ... verbal and group presentation format. + Ability to advocate for regulatory decisions across global cross-functional teams. + Ability to actively listen to… more
- Chemours (Providence, RI)
- …and more modern living depend on Chemours chemistry. Chemours is seeking a ** Director of Regulatory Advocacy** to join our growing Government Affairs team! ... to develop market-leading products with the highest levels of performance, sustainability, and safety in the industry. Powered by chemistry, our products are used in… more
- Charles River Laboratories (Wayne, PA)
- …Biologics Testing Solutions** With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging ... River operations and serves as a member of the Regulatory Affairs and Compliance management team. Provides direction in...administered at the site/operation. ⦁ Direct activities of assigned group (s) to ensure optimum performance of the group… more
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