Regulatory Affairs Expertise in Clinical Materials and Compliance

Regulatory Affairs Professional Role OverviewThis is a key role in the development of cutting-edge structural heart devices, working closely with cross-functional teams to ensure compliance with internal and external regulatory requirements.Key Responsibilities:Clinical:Coordinate and support global clinical trial execution, including site activation,...

Regulatory Affairs ProfessionalThe ideal candidate will have a strong background in regulatory affairs, specifically in medical devices.Main Responsibilities:Develop and implement regulatory strategies to ensure compliance with European and US regulations.Support the creation and maintenance of product design and technical documentation in accordance with...

Support the product development of a cutting-edge structural heart device through design development, verification, clinical trials, validation and regulatory approval.Reporting LinesReports to Clinical and/or Regulatory ManagerKey responsibilities and DutiesClinicalCoordinate and support activities related to global clinical trial execution, including site...

OverviewOur client is a leading Rare Disease biopharmaceutical company committed to advancing innovative treatments to improve patient outcomes. Their mission is to transform care by delivering cutting-edge therapies while fostering strong scientific engagement with healthcare professionals and researchers.Our client is seeking a highly experienced Director...

Job Overview:We are seeking a seasoned Regulatory Affairs professional to lead regulatory support for assigned programs, ensuring sound planning and tactical implementation of US and international regulatory submission strategies.The ideal candidate will have expertise in CMC regulatory strategies, strong collaboration skills, and experience serving as...

Support the product development of a cutting-edge structural heart device through design development, verification, clinical trials, validation and regulatory approval.Reporting LinesReports to Clinical and/or Regulatory ManagerKey responsibilities and DutiesClinical- Coordinate and support activities related to global clinical trial execution, including...

The RoleSupport the product development of a cutting-edge structural heart device through design development, verification, clinical trials, validation and regulatory approval.Reporting LinesReports to Clinical and/or Regulatory ManagerKey responsibilities and DutiesClinicalCoordinate and support activities related to global clinical trial execution,...

Job DescriptionOur company is seeking an experienced Regulatory Affairs Director (Europe) to lead our regulatory strategy and execution across European markets. This key leadership role is responsible for guiding products through clinical development, marketing authorization, and lifecycle management, while serving as the primary regulatory interface with...

Job Title: Global Regulatory Affairs ManagerJob DescriptionThe role of the Global Regulatory Affairs Manager is to develop and implement regulatory strategies that ensure compliance with global regulations. This involves staying up-to-date with changing regulatory requirements, assessing risks, and making informed decisions to mitigate these...

Job Title: Regulatory Affairs SpecialistAbout the Role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team. In this role, you will be responsible for providing expertise and guidance on payments and financial services regulation, as well as stakeholder engagement.Key Responsibilities:Regulatory Compliance: Ensure compliance with...