Regulatory Affairs Manager

Job SummaryClinical Resource Network (CRN) is seeking a highly skilled CMC Regulatory Affairs Manager to join our team. As a key member of our regulatory affairs department, you will be responsible for providing strategic guidance on CMC regulatory matters for investigational, new, and marketing products.Key ResponsibilitiesCMC Regulatory Strategy: Develop...

Job SummaryClinical Resource Network (CRN) is seeking a highly skilled CMC Regulatory Affairs Manager to join our team. As a key member of our regulatory affairs department, you will be responsible for providing strategic guidance on CMC regulatory matters for investigational, new, and marketing products.Key ResponsibilitiesCMC Regulatory Strategy: Develop...

Position: Regulatory Affairs ManagerLocation: Princeton NJ – RemoteJob Description:The task includes supporting necessary submission activities for CTAs under the EU CTR. Essential Duties and Responsibilities: Prepare and submit CTAs within the EU Clinical Trial Integrated System (CTIS) and MHRA Integrated Regulatory Submission (IRAS) submission portals in...

Position: Regulatory Affairs ManagerLocation: Princeton NJ – RemoteJob Description:The task includes supporting necessary submission activities for CTAs under the EU CTR. Essential Duties and Responsibilities: Prepare and submit CTAs within the EU Clinical Trial Integrated System (CTIS) and MHRA Integrated Regulatory Submission (IRAS) submission portals in...

Job SummaryTaiho Oncology, Inc. is seeking a highly skilled Regulatory Affairs Operations Director to join our team. As a key member of our Regulatory Affairs department, you will be responsible for managing global regulatory operational activities for all Taiho Oncology, Inc. projects.Key ResponsibilitiesRegulatory Operations Management: Manage global...

Position: Senior Regulatory Affairs SpecialistLocation: Princeton, NJContract Duration: 12 MonthsExperience Required: 3-5 years in Medical Device Regulatory AffairsEssential Skills:Proficient understanding of EU MDR regulationsKnowledgeable in Regulatory Change AssessmentExperienced with US and EU medical device submission processesBackground in supporting...

Position OverviewThis role is focused on enhancing regulatory compliance within the medical device sector. The successful candidate will collaborate with various departments to refine and advance regulatory processes.Experience Requirements:3-5 years of experience in Medical Device Regulatory Affairs.Proficient understanding of EU Medical Device Regulation...

COME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA EMPLOYEE! Hybrid work arrangement Medical, Dental, Vision Benefits Health Savings Account (HSA), Flexible Spending Account (FSA) Prescription Drug Coverage Telehealth and Behavior Health Services Income Protection – Short Term and Long Term Disability Benefits Retirement Benefits - 401k Company Match on...

Role: Senior Regulatory Affairs SpecialistLocation: Princeton, NJ - 08540Duration: 12 MonthsYears Experience: Must have 3-5 years of experiences in Medical Device Regulatory AffairsSkills:Have working knowledge in EU MDRHave working knowledge in Regulatory Change Assessment inHave working knowledge in US and EU medical device submissionsHave experience...

Job DescriptionJob DescriptionYears Experience: Must have 3-5 years of experiences in Medical Device Regulatory AffairsHave working knowledge in EU MDRHave working knowledge in Regulatory Change Assessment inHave working knowledge in US and EU medical device submissionsHave experience supporting internal and external inspectionsWork cross-functionally and in...

Position: Senior Regulatory Affairs SpecialistCompany: Intellectt IncRole Overview:This role involves collaborating with various departments to enhance and refine regulatory affairs processes. The specialist will support the execution of strategies and operations related to regulatory affairs, which includes overseeing the preparation of product registration...

Role: Senior Regulatory Affairs SpecialistLocation: Princeton, NJDuration: 12 MonthsJob Description: Years’ Experience: Must have 3-5 years of experiences in Medical Device Regulatory AffairsResponsibilities: This position will be working with multiple business units to develop, update, and improve regulatory affair processes. Assist the strategy...

Job Details:Role: Senior Regulatory Affairs SpecialistLocation: Princeton, NJ - 08540Duration: 12 MonthsYears Experience: Must have 3-5 years of experiences in Medical Device Regulatory AffairsSkills:Have working knowledge in EU MDRHave working knowledge in Regulatory Change Assessment inHave working knowledge in US and EU medical device submissionsHave...

Job Details:Role: Senior Regulatory Affairs SpecialistLocation: Princeton, NJ - 08540Duration: 12 MonthsYears Experience: Must have 3-5 years of experiences in Medical Device Regulatory AffairsSkills:Have working knowledge in EU MDRHave working knowledge in Regulatory Change Assessment inHave working knowledge in US and EU medical device submissionsHave...

Position: Senior Regulatory Affairs SpecialistCompany: Intellectt IncKey Responsibilities:Engage with various departments to refine and enhance regulatory affairs methodologies.Support the execution of strategies and operations related to regulatory affairs, encompassing product registration submissions, status updates, and modifications.Revise and formulate...

Position: Senior Regulatory Affairs SpecialistCompany: Intellectt IncRole Overview: The Senior Regulatory Affairs Specialist will play a crucial role in overseeing and enhancing regulatory processes within the organization.Key Responsibilities:Engage with various departments to refine and improve regulatory affairs methodologies.Support the execution of...

Position: Senior Regulatory Affairs SpecialistCompany: Intellectt IncRole Overview: The Senior Regulatory Affairs Specialist will play a pivotal role in ensuring compliance with regulatory standards and enhancing operational processes within the organization.Key Responsibilities:Engage with various departments to refine and advance regulatory affairs...

Role: Senior Regulatory Affairs Specialist Location: Princeton, NJ 08540 Duration: 12 MonthsKey Responsibilities:Collaborate with multiple business units to develop, update, and enhance regulatory affairs processes.Assist in strategy implementation and operations for regulatory affairs, including product registration submissions, progress reports, and...

Role: Senior Regulatory Affairs Specialist Location: Princeton, NJ 08540 Duration: 12 MonthsKey Responsibilities:Collaborate with multiple business units to develop, update, and enhance regulatory affairs processes.Assist in strategy implementation and operations for regulatory affairs, including product registration submissions, progress reports, and...

Job SummaryThe Director, Global Regulatory Lead will be responsible for leading the development and execution of regulatory strategies for assigned brand programs. This role will provide strategic, tactical, and operational direction and guidance for product's pipeline and key regulatory milestones.Key ResponsibilitiesServe as key corporate regulatory...