LAVORO REGULATORY AFFAIRS PHARMA CRO
(38 offerte di lavoro)
Listado de trabajos de Regulatory affairs pharma cro
Regulatory affairs project specialist - system implementation
Are you passionate about regulatory compliance, business growth and project management? we are looking for a dynamic senior regulatory affairs specialist to lead...
Junior regulatory affairs associate
Torbay pharma are currently recruiting for a junior regulatory affairs associate to join our team, in devon, on a permanent basis... what you can expect in a junior...
Requirements: proven experience in regulatory affairs within an api manufacturing environment... oversee responses to deficiency letters from regulatory authorities...
Regulatory affairs specialist ii
Randstad inhouse services, divisione specializzata di randstad italia spa, specialty pharma ricerca per importante azienda multinazionale del settore chimico farmaceutico:...
Regulatory affairs middle - bologna
Your roleregulatory affairs specialist - bologna (bo) in capgemini engineering, leader mondiale nei servizi di ingegneria, uniamo un team globale di ingegner*, scienziat*...
Job title: director regulatory strategy, cmc, italy - p
Keywords: director regulatory strategy, director regulatory strategy, cmc, senior manager regulatory strategy, cmc, cmc regulatory affairs, cmc regulatory...
Senior director, global regulatory affairs-emea
Model the innovation, leadership behaviors and regulatory excellence attributes as described in global regulatory affairs white papers... contribute during key governance...
Director, business development – iqvia regulatory clinical services - 1 year assignment
Requirements possess an understanding of the regulatory affairs and pharmacovigilance processes for both pre-marketed and post-marketed stages of a product selling...
Contractor regulatory operations associate
Main point of contact for globalchemistry manufacturing&controls (gcmc) dpt or local regulatory affairs in pfizer country offices (single market prods) for the regulatory...
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Contractor regulatory operations associate
Main point of contact¿for globalchemistry¿manufacturing&controls¿(gcmc)¿dpt¿or¿local regulatory affairs in¿pfizer country offices (single market prods) for¿the¿regulatory...
Associate director/director, gra-emea
Model the innovation, leadership behaviors and regulatory excellence attributes as described in global regulatory affairs white papers... com/us/en/workplace-accommodation)...
Medical director, clinical development - psychosis spectrum illness
Required technical knowledge and skills: experience/ expertise in in experimental medicine-based early human studies that confirm mechanism of action, pharmacology...
External supply operations quality manager (fixed term contract)
Main point of contact for global chemistry manufacturing & controls (gcmc) dpt or local regulatory affairs in pfizer country offices (single market prods) for the...
Job title: clinical research associate (cra ii/scra), italy - l
Skills: cardiology, oncology, respiratory, clinical research associate, clinical trials, cro, medical devices, monitoring, pharma location: italy...
Director, medical excellence strategy (hematology)
Qualifications education: bachelor's degree md, pharmd, phd, and/or mba, preferred required: a minimum of 8 years in the pharma industry or adjacent fields, with...
Job title: senior clinical project manager, italy - p
A minimum of 3 years of experience with a cro is needed... you will work on projects from our varied client base, ranging from small to mid-sized pharma and medical...
Global r&d qa, senior documentation specialist
Experience required at least 3 years experience within r&d in a pharma company, particularly in quality & compliance groups... support qualified persons in the...
Real world evidence study manager - temporary
Processes and tools support the implementation and specific adaptation of procedures within rwe studies fulfil regulatory requirements and company strategic...
Senior clinical research associate (m/f/d)
Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out... works in partnership internally with...
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