TRABAJO DIRECTOR GLOBAL REGULATORY SCIENCES BARCELONA, BARCELONA
(36 ofertas de trabajo)
Listado de trabajos de Director global regulatory sciences en Barcelona, Barcelona
Regulatory affairs management director, regulatory science & execution
Drive knowledge management by sharing case studies/lessons learned from regulatory activities within the regulatory science & execution...
Cmc regulatory affairs director
This role will represent cmc in networks across the business including pharmaceutical development project teams, global regulatory strategy teams, global supply...
Global development medical director
Lead and contribute to medical monitoring of trials provide expert medical input into the preparation of regulatory documents and interactions with regulatory authorities...
Global marketing lead/director, solgar
The global marketing lead/director, solgar will lead the development and implementation of brand-building consumer initiatives and marketing campaigns for solgar...
Director, global scientific communications, metabolics plus, hypoparathyroidism
The director will chair the respective metabolic ta global publications team as well as engage with cross-functional partners including but not limited to research...
Associate director, business analyst, ddit dev., regulatory affairs
Experience in regulatory affairs business processes is a plus (e... we are looking for an experienced individual in global drug development regulatory affairs to...
Treasury director - global (they/she/he)
Ensure compliance with treasury policies, procedures, and regulatory requirements... establish and maintain strong relationships with global banking partners to...
Cmc regulatory affairs manager
With our expertise, we interpret, anticipate, and shape global health authority expectations to build insightful cmc and device regulatory strategies...
Medical device regulatory & quality consultant
Documentation preparation: prepare comprehensive regulatory documentation for medical devices, including ivds and medical device software, ensuring compliance with...
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Global market development project manager - rhinology & gastroenterology - vie contract
As global market development project manager - rhinology & gastroenterology vie in our global dupixent team, you’ll participate in the implementation of market...
Associate director, biostatistics
You will be responsible for: the associate director, biostatistics may work as a lead statistician: for a project or indication in clinical or preclinical therapeutic...
Senior director, biostatistics
This includes development plans, regulatory strategy and submissions, high level internal governance committees, health technology assessment and reimbursement/payer...
Specialist cmc regulatory affairs (big pharma)
Requirements:academic background in life sciences... work closely with regulatory to develop effective regulatory and cmc strategies... experience in qa and ra departments...
Associate director, medical communications and information
The associate director, medical communications & information, is accountable for the execution of us & global mc&i brand/therapeutic area deliverables...
Director, digital health implementation, digital health r&d
Thoughtful risks and quick decisions come together to accelerate innovation across the life sciences sector... · ability to work in a global environment including...
Associate director, clinical development scientist
The person in this position may provide input into the global clinical development plans and strategy for cellular therapy in al amyloidosis...
Director, precision medicine oncology
Delivery of companion diagnostics, regulatory interactions and commercialisation... leading companion diagnostic regulatory interactions to secure companion diagnostic...
Lead the local upskilling of rwe with global initiatives, events and learning opportunities, coordinated with the global upskilling in rwe strategic initiative...
Stephen rhodes, director... keywords:senior project manager pharma pharmaceutical life sciences saas ai manufacturing cdmo gmp gxp ebr scada lims mes industry 4...
Senior study start up associate
Strong understanding of regulatory requirements and guidelines for clinical trials, including ich-gcp and local regulatory requirements... in addition to your competitive...
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