Regulatory Affairs Director

Director of Regulatory Affairs and Clinical TrialsWe are seeking a highly experienced Director to lead our regulatory affairs and clinical trials team.About the RoleThis is a senior leadership position that will oversee the strategic direction of our regulatory affairs and clinical trials operations.Key ResponsibilitiesProvide strategic guidance on...

Unlock Your Potential in Regulatory AffairsAt Parexel, we're seeking a highly skilled Regulatory Affairs professional to join our team. As a Regulatory Affairs Director, you will play a critical role in ensuring the success of our clinical trials by providing expert guidance on regulatory submissions and compliance.10+ years of experience in Clinical Trial...

**About Lifelancer**Lifelancer is a global talent-hiring platform that connects professionals with opportunities in the life sciences, pharma, and IT industries. Our goal is to help individuals advance their careers while promoting equal opportunities for people with disabilities. **Company Overview**Lilly is a global healthcare leader headquartered in...

About the RoleParexel is seeking a skilled Senior Regulatory Affairs Director to lead clinical trial regulatory submissions and regulatory leadership initiatives. As a key member of our team, you will be responsible for managing clinical trial studies, serving as the regulatory lead for global trials, and providing guidance to project team members.Clinical...

Regulatory Affairs ManagerAt Parexel, we're driven by a shared passion for delivering exceptional results. When our values align, there's no limit to what we can achieve.10+ years of relevant experience in Clinical Trial Regulatory SubmissionsExperience in managing clinical trial studies, playing Regulatory Leads for Global trials, and exposure to the...

Empowering Excellence in Regulatory Affairs At Parexel, we are committed to delivering exceptional results and quality services. As an Associate Director of Regulatory Affairs, you will play a critical role in ensuring the success of our clinical trials and regulatory submissions. Key Responsibilities Clinical Trial Regulatory Submissions : Over 15...

Key ResponsibilitiesAs a key member of our team, you will be responsible for ensuring the successful execution of clinical trials by providing regulatory expertise and guidance.Clinical Trial Regulatory Submissions: Develop and implement regulatory strategies for clinical trials, ensuring compliance with relevant regulations and guidelines.Regulatory...

About the RoleWe are seeking a highly experienced Regulatory Affairs Director to join our team at Parexel. As a key member of our regulatory team, you will be responsible for leading clinical trial regulatory submissions and providing regulatory leadership for global trials.Key ResponsibilitiesClinical Trial Regulatory Submissions: Over 15 years of relevant...

About the RoleParexel is seeking a highly experienced Regulatory Affairs Director to lead our clinical trial regulatory submissions team. As a key member of our team, you will be responsible for managing global trials, ensuring compliance with regulatory requirements, and providing guidance to project teams.Key ResponsibilitiesClinical Trial Regulatory...

About this roleWe are seeking a highly experienced Regulatory Affairs Director to join our team at Parexel. As a key member of our regulatory team, you will be responsible for ensuring the successful submission of clinical trial regulatory documents.Key ResponsibilitiesClinical Trial Regulatory Submissions: Over 15 years of relevant experience in clinical...

Regulatory Affairs SpecialistAt Parexel, we're seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for managing the regulatory life cycle of drug products, from pre-approval to post-approval. Your expertise will be essential in ensuring compliance with regional regulatory...

Regulatory Affairs at Baxter: A Key Role in Delivering Innovative Healthcare SolutionsBaxter, a leading medical products company, is seeking a talented Regulatory Affairs Specialist to join its team. In this crucial role, you will play a key part in ensuring the company's products meet the highest regulatory standards, enabling us to deliver innovative...

Job Title: Sr. Regulatory Affairs SpecialistYou will be an integral member of our Clinical Informatics Regulatory Affairs team, influencing and shaping the regulatory capabilities for future success of Philips.Your Key Responsibilities:Ensure safe and effective products/solutions are brought to market on time and sustained throughout their lifecycle via...

Job Title: Manager Global Regulatory AffairsAt Biocon Biologics, we are seeking a highly skilled and experienced Manager Global Regulatory Affairs to join our team.Key Responsibilities:Develop and execute global regulatory strategies for biosimilar products, ensuring compliance with regulatory requirements and industry standards.Collaborate with...

Company OverviewLifelancer is a leading talent-hiring platform in the Life Sciences, Pharma, and IT sectors. Our mission is to connect top talent with opportunities in these fields. Job Title: Regulatory Affairs ManagerSalary: $120,000 - $180,000 per yearLocation: Remote or On-Site (Flexible)Job Description:We are seeking an experienced Regulatory Affairs...

Job Title: Regulatory Affairs LeadAt Indegene, we are seeking a highly skilled Regulatory Affairs Lead to join our team. This role will be responsible for ensuring compliance with regulatory requirements for medical devices worldwide.Key Responsibilities:Disseminate regulatory intelligence and coordinate with stakeholders to ensure compliance.Assess...

About the RoleParexel is seeking a highly skilled Regulatory Affairs professional to join our team. As a Regulatory Affairs Consultant, you will be responsible for managing the pre- and post-approval life cycle of biologic products in various markets, including regulated (EU/US/Canada) and emerging markets.Key ResponsibilitiesDevelop and implement regulatory...

The Regulatory Affairs function at ResMed plays a crucial role in ensuring compliance with regulatory frameworks and delivering optimal regulatory strategies for portfolio planning, active regulatory intelligence, and excellence in execution.Key Responsibilities:Support and maintain various internal and government databases relevant to ResMed's...

About VantiveVantive is a new company built on the legacy of Baxter, a leading healthcare company. We are on a mission to revolutionize kidney care and other vital organ support.Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team. The successful candidate will be responsible for supporting all regulatory activities...

Regulatory Affairs LeadThe ideal candidate for this role will be a highly organized and detail-oriented individual with a strong background in Medical Device Regulations. As a Regulatory Affairs Lead at Indegene, you will be responsible for ensuring compliance with global regulations and facilitating the registration of medical devices.Key...