TRABAJO CLINICAL REGULATORY AFFAIRS LEAD CAÑADA, ALICANTE
(9 ofertas de trabajo)
Listado de trabajos de Clinical regulatory affairs lead en Cañada, Alicante
Associate director, regulatory affairs
Collaborate with global regulatory teams and the global regulatory affairs (gra) function/teams to facilitate regulatory activities... the associate director, regulatory...
Collaborate with global cross-functional teams and the global regulatory affairs (gra) function/teams to facilitate regulatory activities... minimum 5 years of pharmaceutical...
Analyst ii, regulatory medical writing
Participate in and may lead cross-functional document planning and review meetings... if a lead writer for a compound or document: primary point of contact and champion...
Medical communications manager (1 of 2)
They will lead the development and execution of the localized, therapeutic area(s) and associated product(s) specific, cross-functional medical communications plans...
Evidence generation operations manager (fixed employee contract)
Proven leadership skills and ability to lead diversified team and stakeholders... scientific and technical thought leadership with knowledge or learning agility...
Manager, global labeling product leader
regulatory affairs, clinical, medical information, pharmacovigilance) an understanding of pharmaceutical drug development experience in discussing and communicating...
Health economics market access manager, orthopaedics
Proven expertise in economic modeling, statistical analysis, and clinical data interpretation... monitor and analyze market trends, competitor activities, and regulatory...
Demand planner (contract role)
Locally, you will work cross-functionally with supply planning, sales, marketing, marketing operation, finance, customer service, regulatory & quality...
Medical science intern - gastroenterology
The internship will give you the chance to support and lead medical science projects... key responsibilities: perform deep scientific dives in immunology therapeutic...
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