TRABAJO GLOBAL REGULATORY SUBMISSIONS PROJECT BARCELONA, BARCELONA
(69 ofertas de trabajo)
Listado de trabajos de Global regulatory submissions project en Barcelona, Barcelona
Clinical project support specialist
provide expertise and support project planning, project management and implementation of functional initiatives to improve processes... -provide updates/reports...
Director, clinical regulatory writing
Typical accountabilities the clinical regulatory writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory...
Medical device regulatory & quality consultant
Experience in project management and auditing is highly valuable... documentation preparation: prepare comprehensive regulatory documentation for medical devices...
Etmf project manager - trial interactive
Transperfect has global headquarters in new york, with regional headquarters in london and hong kong... more than global organizations employ transperfect’s globallink®...
Global study associate director late oncology
Proven project management experience on a global level... the global study associate director (gsad) is responsible for the delivery of clinical studies, including...
Global clinical operations program director - haematology
What you’ll do the global clinical operations program director (gpd) is a core global role within the haematology r&d clinical operations function...
Associate director, safety scientist, global patient safety
This is what you will do: the associate director, safety scientist plays a leadership role within global patient safety (gps) to actively evaluate and manage risk...
Regulatory affairs manager [interim maternity]
Rims) for regulatory processes... oxford global resources is seeking a regulatory affairs manager for a 6-month interim project to support a leading company headquartered...
Global accounting and reporting analyst (m/f/d)
• participate in global finance projects as project manager, coordinator, orcontributor... • liaise between global business services and the business/controllingcommunity...
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Global market access academy specialist - vie contract
Strong project management skills including quality standards... lead and manage learning & development projects (career development, specific market access topics)...
Global pricing implementation lead oncology
The purpose of this role is to optimize the implementation of price & market access strategies of az brands by supporting reimbursement decisions at a local, regional...
Global program safety lead - immunology
regulatory compliance... regulatory and professional inquiries: respond to inquiries from regulatory authorities or healthcare professionals regarding safety issues...
Head of global hr systems and governance (m/f/d)
Worked in global environments... project management skills, knowledge of hris and regulatory compliance... hr pmo / monitor project progress and report on key metrics...
Associate director scientist, early oncology global development
Supports the physician/senior clinical scientist in representing the project internally and externally with key external experts... other: based on areas of expertise...
Regulatory & quality mdr -temporal-
At oxford global resources, we are looking for a regulatory affairs jr... assisting in identifying and resolving any gaps in compliance, in collaboration with the...
Senior global study manager onco (temp big pharma)
Astrazeneca is looking for a clinical project manager for its global hub in barcelona for a temporary contract... direct the study team in the implementation of...
Senior project developer *italian speaking*
Keep a close eye on industry trends/ updates and regulatory frameworks and rectify work where necessary... italian speaking senior project developer – spain - €excellent...
Cybersecurity solutions architect (global drug development team)
The successful candidate will be a strong communicator with deep technical and security skills, especially pertaining to regulatory and gxp systems used in the pharmaceutical...
Senior manager, nonclinical and clinical pharmacology writing
Experience with global clinical studies and regulatory submissions... thorough knowledge of global regulatory requirements and ich/gcp guidelines...
Director, nonclinical and clinical pharmacology writing
Broad experience with global clinical studies and regulatory submissions... thorough knowledge of global regulatory requirements and ich/gcp guidelines...
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