Regulatory Affairs Consultant
hace 3 semanas
We are seeking a highly skilled Regulatory Affairs Consultant to join our Clinical and Regulatory Team at Clarivate. As a key member of our team, you will be responsible for delivering high-quality regulatory services to our global clients.
Key Responsibilities:
- Project Delivery Support: Act as a point of contact for customers throughout a project's lifecycle, ensuring successful delivery of each assigned project.
- Business Development: Support Requests for Information (RFIs) and Requests for Proposals (RFPs), providing robust effort estimates for scoped projects.
- Quality Management System (QMS) Implementation: Set up, maintain, and certify readiness for QMS systems.
- Audit and Inspection Management: Perform and receive audits from Certification Bodies and Competent Authorities.
About the Team:
The Clinical and Regulatory Consulting Team works towards adding value to data from different sources and providing professional regulatory services to our global clients. We demonstrate good networking skills and establish rapport with clients and internal/external stakeholders.
What We Offer:
- A modern culture environment combined with financial and stability advantages of working for a large business.
- Active volunteering community with 40 annual paid hours of volunteering time.
- Private Health and Life & Disability insurances.
- Tax-free benefits, language classes, and a global and dynamic employee base.
Requirements:
- Bachelor's or Master's degree in pharmaceutical sciences.
- At least 5 years of relevant work experience in quality affairs & regulatory affairs or in supporting quality & regulatory professional services/consulting projects.
- Exposure to regulatory consulting, customer-facing or customer-service experience, and Master's degree in regulatory & quality affairs.
Working Conditions:
This is a permanent full-time position at 40 hours a week (35 hours during July and August). The working schedule is flexible, mostly centered on CET time zone with the occasional need to accommodate late or early meetings with US or East Asia time zones. The position is hybrid, going to the office in Barcelona 2-3 times per week.
-
Regulatory Affairs Consultant
hace 4 semanas
Barcelona, Barcelona, España Clarivate A tiempo completoAbout the RoleWe are seeking a highly skilled Regulatory Affairs Consultant to join our Clinical and Regulatory Team at Clarivate. As a key member of our team, you will be responsible for delivering regulatory consulting projects and supporting business development initiatives.Key ResponsibilitiesProject Delivery Support (70%): Act as a point of contact for...
-
Regulatory Affairs Consultant
hace 4 semanas
Barcelona, Barcelona, España Clarivate A tiempo completoAbout the RoleWe are seeking a highly skilled Regulatory Affairs Consultant to join our Clinical and Regulatory Team at Clarivate. As a key member of our team, you will be responsible for delivering regulatory consulting projects and supporting business development initiatives.Key ResponsibilitiesProject Delivery Support (70%): Act as a point of contact for...
-
Regulatory Affairs Specialist
hace 4 semanas
Barcelona, Barcelona, España Ramboll Group AS A tiempo completoJoin Ramboll's International Team as a Regulatory Affairs ConsultantWe are seeking a highly skilled Regulatory Affairs Consultant to join our international team in Spain. As a key member of our Health Sciences service line, you will play a crucial role in supporting clients across various industries, ensuring compliance with European regulations and product...
-
Regulatory Affairs Specialist
hace 4 semanas
Barcelona, Barcelona, España Ramboll Group AS A tiempo completoJoin Ramboll's International Team as a Regulatory Affairs ConsultantWe are seeking a highly skilled Regulatory Affairs Consultant to join our international team in Spain. As a key member of our Health Sciences service line, you will play a crucial role in supporting clients across various industries, ensuring compliance with European regulations and product...
-
Regulatory Affairs Specialist
hace 4 semanas
Barcelona, Barcelona, España Ramboll Group AS A tiempo completoUnlock Your Expertise in Regulatory AffairsWe're seeking a talented Regulatory Affairs Consultant to join our global team at Ramboll Group A/S. As a key member of our Health Sciences service line, you'll play a crucial role in supporting organizations around the world in bringing products to market that meet regulatory requirements and prioritize human...
-
Regulatory Affairs Specialist
hace 4 semanas
Barcelona, Barcelona, España Ramboll Group AS A tiempo completoUnlock Your Expertise in Regulatory AffairsWe're seeking a talented Regulatory Affairs Consultant to join our global team at Ramboll Group A/S. As a key member of our Health Sciences service line, you'll play a crucial role in supporting organizations around the world in bringing products to market that meet regulatory requirements and prioritize human...
-
Regulatory Affairs Consultant
hace 3 semanas
Barcelona, Barcelona, España Clarivate A tiempo completoWe are seeking a highly skilled Regulatory Affairs Consultant to join our Clinical and Regulatory Team at Clarivate. This is an exciting opportunity to work on regulatory and quality consulting projects, leveraging your expertise in quality regulatory affairs and consulting domain.About the RoleThe successful candidate will be responsible for project...
-
Barcelona, Barcelona, España Primevigilance A tiempo completoJob DescriptionThis is an exciting opportunity for a freelancer/consultant to join our team as a Local Contact Person for Pharmacovigilance and Regulatory Affairs at 0.5 FTE.Main ResponsibilitiesPrimary contact person for local regulatory authority/Pharmacovigilance expert as per local requirementsPrompt and effective communication with local regulatory...
-
Barcelona, Barcelona, España Primevigilance A tiempo completoJob DescriptionThis is an exciting opportunity for a freelancer/consultant to join our team as a Local Contact Person for Pharmacovigilance and Regulatory Affairs at 0.5 FTE.Main ResponsibilitiesPrimary contact person for local regulatory authority/Pharmacovigilance expert as per local requirementsPrompt and effective communication with local regulatory...
-
Regulatory Affairs Director
hace 3 semanas
Barcelona, Barcelona, España Innovaderm Research A tiempo completoThe Senior Manager, Regulatory Affairs will lead the regional regulatory affairs department at Innovaderm Research, ensuring all services are conducted according to standard operating procedures, applicable regulations, and good clinical practices. Key responsibilities include providing leadership on regulatory activities, planning and assigning work,...
-
Regulatory Affairs Specialist
hace 4 semanas
Barcelona, Barcelona, España Lhh A tiempo completoDescripción del PuestoBuscamos un Regulatory Affairs Consultant para unirse a nuestra división de LifeSciences de LHH Recruitment Solutions.ResponsabilidadesPreparar la documentación necesaria para obtener el marcado CE, FDA o registros de otros países según la legislación vigente.Gestionar diversos proyectos de Regulatory para diferentes clientes del...
-
Regulatory Affairs Specialist
hace 4 semanas
Barcelona, Barcelona, España Lhh A tiempo completoDescripción del PuestoBuscamos un Regulatory Affairs Consultant para unirse a nuestra división de LifeSciences de LHH Recruitment Solutions.ResponsabilidadesPreparar la documentación necesaria para obtener el marcado CE, FDA o registros de otros países según la legislación vigente.Gestionar diversos proyectos de Regulatory para diferentes clientes del...
-
Regulatory Affairs Specialist
hace 3 semanas
Barcelona, Barcelona, España Galderma Pharma S.A A tiempo completoJob Title:Regulatory Affairs SpecialistGalderma Pharma S.A is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.The ideal candidate will have a strong...
-
Regulatory Affairs Director
hace 3 semanas
Barcelona, Barcelona, España Innovaderm Research A tiempo completoJob SummaryThe Senior Manager, Regulatory Affairs will lead the regional regulatory affairs department to ensure compliance with Innovaderm's standard operating procedures, applicable regulations, and good clinical practices. Key responsibilities include providing strategic guidance on regulatory activities, overseeing the performance of direct reports, and...
-
Regulatory Affairs Specialist
hace 3 semanas
Barcelona, Barcelona, España Galderma A tiempo completoAt Galderma, we're seeking a talented Regulatory Affairs Strategist to join our team in Barcelona, Spain. As a key member of our Global R&D team, you'll be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.The ideal candidate will have a strong background in regulatory...
-
Regulatory Affairs Specialist
hace 3 semanas
Barcelona, Barcelona, España Alk-Abelló AS A tiempo completoJob Title: Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Alk-Abelló A/S. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with regulatory requirements and ensuring the smooth submission of CMC documentation for Marketing Authorisation...
-
Regulatory Affairs Specialist
hace 4 semanas
Barcelona, Barcelona, España Mcr International A tiempo completoRegulatory Affairs ManagerMcr International is seeking a highly skilled Regulatory Affairs Manager to join our team. As a key member of our regulatory department, you will be responsible for designing and implementing regulatory strategies to drive business growth and maintain compliance in the South Cluster.Key Responsibilities:Develop and execute...
-
Regulatory Affairs Specialist
hace 4 semanas
Barcelona, Barcelona, España Mcr International A tiempo completoRegulatory Affairs ManagerMcr International is seeking a highly skilled Regulatory Affairs Manager to join our team. As a key member of our regulatory department, you will be responsible for designing and implementing regulatory strategies to drive business growth and maintain compliance in the South Cluster.Key Responsibilities:Develop and execute...
-
Regulatory Affairs Specialist
hace 2 meses
Barcelona, Barcelona, España Galderma A tiempo completoRegulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating CMC dossier sections for assigned products.Key Responsibilities:Contribute to global regulatory CMC strategiesAssess regulatory impact...
-
Regulatory Affairs Specialist
hace 2 meses
Barcelona, Barcelona, España Galderma A tiempo completoRegulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating CMC dossier sections for assigned products.Key Responsibilities:Contribute to global regulatory CMC strategiesAssess regulatory impact...