Regulatory Strategy Jobs in Waltham, MA

The Director Oncology Business Development and Global Regulatory Strategy is responsible for developing and implementing globalstrategies to secure and maintain market approval for product(s) in the assigned therapeutic area.   Leads the Global Regulatory Product Team ( More...

The Director Regulatory Affairs Global Regulatory Lead Global Regulatory Strategy is responsible for developing and implementing globalstrategies to secure and maintain market approval for product(s) in the assigned therapeutic area.   Leads the Global Regulatory Product Tea More...

Job DescriptionJob Summary:The Manager (contractor) will be part of Analytical Science and Technology (ASAT) team within Commercial Manufacturing & Supply Chain (CMSC) department. S/He/They will provide support with development and of the analytical CMC strategy by contributing t More...

The Director Oncology Business Development and Global Regulatory Strategy is responsible for developing and implementing globalstrategies to secure and maintain market approval for product(s) in the assigned therapeutic area.   Leads the Global Regulatory Product Team ( More...

Key Responsibilities: Provide input to global regulatory submission strategy preparing regulatory submission documents and reviewing regulatory submissions for completeness and quality in global accordance with regulatory agency requirements standards and corporate practicesPrevious e More...

Work ScheduleStandard (MonFri)Environmental ConditionsOfficeJob DescriptionWhen youre part of the team at Thermo Fisher Scientific youll do important work. And youll have the opportunity for continual growth and learning in a culture that empowers your development. With revenues of mo More...

The Director Regulatory Affairs Global Regulatory Lead Global Regulatory Strategy is responsible for developing and implementing globalstrategies to secure and maintain market approval for product(s) in the assigned therapeutic area.   Leads the Global Regulatory Product Tea More...

COMPANY DESCRIPTIONSynerG BioPharma Group and Sequoia Biotech Consulting recently merged in September 2024 uniting two industry leaders to create a new force in life sciences consulting. By combining our expertise in product development regulatory strategy quality and compliance and c More...

About This RolePharmacometric analyses and insight are critical in the development of drug candidates determination of product viability and maximization of commercial value at Biogen.  As the Director Pharmacometrics you have responsibility for high priority clinical development More...

Job Title: Mgr Regulatory Affairs Pharma HealthCanada Job Location: Waltham MA USA Job Location Type: Remote Job Contract Type: Fulltime Job Seniority Level: MidSenior level PURPOSE AND SCOPE: Ensure overall (other than auditing responsibilities) regulatory compliance for FMCNA phar More...

Single point of contact/single point of accountability within GRA on the Core Asset Team (CTA) and Medicines Development Team (MDT) for assigned program(s)Chairs a Global Regulatory Team (GRT) of regulatory Subject Matter Expert(s)Provides global regulatory leadership of assigned prog More...

PurposeDescribe the primary goals objectives or functions or outputs of this position.Leads global regulatory dossier preparation activities by coordinating crossfunctional teams of subject matter experts from internal and external third parties. The primary function is to ensure cons More...