Regulatory Contracts Specialist

Job Title: Regulatory Contracts Coordinator/SpecialistLocation: Cambridge, MA (Hybrid)Therapeutic Area: Rare DiseaseJob Overview: This position is responsible for overseeing the regulatory contract process, from negotiating agreements and vendor setup to ensuring compliance and handling all related documentation.Key Responsibilities:Negotiate and manage...

Job Title: Regulatory Contracts Coordinator/SpecialistLocation: Cambridge, MA (Hybrid)Therapeutic Area: Rare DiseaseJob Overview: This position is responsible for overseeing the regulatory contract process, from negotiating agreements and vendor setup to ensuring compliance and handling all related documentation.Key Responsibilities:Negotiate and manage...

Job OverviewWe are seeking a highly skilled Regulatory Contracts Coordinator/Specialist to join our team at Stratacuity: Proven Scientific Placement. This role will be responsible for overseeing the regulatory contract process, from negotiating agreements and vendor setup to ensuring compliance and handling all related documentation.Key...

Job OverviewWe are seeking a highly skilled Regulatory Contracts Coordinator/Specialist to join our team at Stratacuity: Proven Scientific Placement. This role will be responsible for overseeing the regulatory contract process, from negotiating agreements and vendor setup to ensuring compliance and handling all related documentation.Key...

Job Title: Regulatory Contracts Coordinator/SpecialistThis role is responsible for overseeing the regulatory contract process, ensuring compliance, and handling related documentation.Key Responsibilities:Negotiate and manage service agreements.Assess and amend contracts based on performance.Coordinate contract compliance and document...

Location: Cambridge, MA (Hybrid)Therapeutic Area: Rare DiseaseJob Overview: As a key member of our team, you will be responsible for overseeing the regulatory contract process, from negotiating agreements and vendor setup to ensuring compliance and handling all related documentation.Primary Job Responsibilities:Develop and implement contract negotiation...

Job Title: Regulatory Affairs SpecialistBeam Therapeutics Inc. is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will play a critical role in ensuring the success of our global regulatory submissions.Key Responsibilities:Prepare and compile documentation packages for global regulatory...

Contract Operations ManagerInternational Staff Consulting is seeking a highly skilled Contract Operations Manager to join our team. As a key member of our Contracts function, you will be responsible for managing and coaching a team of Contracts Specialists, creating and implementing processes to mitigate risk and improve efficiency, and ensuring compliance...

Company Overview:Beam Therapeutics Inc. is a pioneering biotech company dedicated to developing innovative genetic medicines. Our mission is to establish a leading platform for precision genetic therapies, leveraging cutting-edge gene editing technologies to address serious diseases.Position Overview:The Regulatory Specialist will play a crucial role in...

Company OverviewBeam Therapeutics Inc. is a pioneering biotech company dedicated to revolutionizing the field of precision genetic medicines. Our mission is to establish a leading platform for gene editing and delivery technologies, enabling the development of innovative treatments for serious diseases.We have assembled a cutting-edge platform that includes...

Job Title: Principal Ultrasound Regulatory Affairs SpecialistAt Philips, we are seeking a highly skilled Principal Ultrasound Regulatory Affairs Specialist to join our team. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the compliance of our ultrasound devices with global regulatory requirements.Key...

Job Title: Principal Ultrasound Regulatory Affairs SpecialistThe Principal Regulatory Affairs Specialist will play a pivotal role in developing comprehensive regulatory strategies for complex new devices and post-market changes within Philips' Ultrasound business.Your Key Responsibilities:Lead business-critical new product development projects, ensuring...

Senior Director, Regulatory StrategyProclinical Staffing is seeking a seasoned professional to lead the development and execution of regulatory strategies for a global biotech company. The ideal candidate will have a strong background in regulatory affairs, with a focus on vaccine development and mRNA platform technology.Key Responsibilities:The Senior...

Job Title: Contracts Operations ManagerInternational Staff Consulting is seeking a highly skilled Contracts Operations Manager to join our team. As a key member of our Contracts function, you will be responsible for managing and coaching a team of Contracts Specialists, creating and implementing processes to mitigate risk and improve efficiency, and ensuring...

Job Title: Contract SpecialistPhilips is seeking a skilled Contract Specialist to join our dynamic team in Cambridge, MA. As a Contract Specialist, you will play a critical role in operationalizing contract requirements in various systems to support market-to-cash processes.Your Role:Implement and manage commercial contracts in SAP, Siebel, and Apttus cradle...

About the RoleAt Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. We are seeking a highly skilled and experienced Regulatory Affairs professional to join our team as an Associate Director, Global Reg Affairs Device, PDT in our Global Regulatory Affairs CMC & Device...

**About the Role**The Compliance Specialist is a key member of the LexisNexis Risk Solutions FL Inc. Company team, responsible for ensuring regulatory compliance across various jurisdictions in the United States. This role involves working closely with a manager to review and submit notice filings on behalf of funds and other investment products. The...

Job SummaryWe are seeking a highly skilled Senior Manager, CMC Facilities Regulatory Affairs to join our team. This role will be responsible for regulatory submissions, interactions with FDA, and strategy for various US vaccines regarding manufacturing facilities and equipment aspects.Key Responsibilities:Act as the legal agent for CMC Facility specific...

Job DescriptionTakeda is a global pharmaceutical company committed to delivering innovative therapies to patients worldwide. We are seeking a highly skilled Director, GRA CMC Small Molecules to join our team.Key ResponsibilitiesDevelop and execute regulatory CMC development and registration strategies for assigned products.Lead cross-functional teams to...

About the RoleWe are seeking a highly experienced and strategic Contracts Management Leader to join our team at Philips in North America. As a key member of our leadership team, you will be responsible for developing and implementing contract strategies that drive business growth and customer satisfaction.Key ResponsibilitiesDevelop and execute contract...