TRABAJO REGULATORY AFFAIRS SPECIALIST MEDICAL BARCELONA, BARCELONA

Overview are you interested in a career in r&d in pepsico? then now is the time to explore the opportunities of pepsico: join us as the next regulatory affairs specialist...

At least 3 years of experience in regulatory affairs with good knowledge of flavor, food or chemical regulations, safety data sheets and database systems...

Parets del vallès (barcelona)empresa: grifolsjornada: completacontrato: indefinido...

Principal responsibilities medical review works collaboratively and develops good working relationships with the global medical affairs lead (gmals) and medical...

Ensures best practices are shared within global regulatory... this role is the key account manager for the regulatory eu marketing company (eumc) thereby managing...

More than 10 years of regulatory affairs experience experience in global regulatory strategy and submissions that have progressed through to registration...

Importante multinacional farmacéutica con site en los alrededores de barcelona, precisa incorporar en su equipo de regulatory affairs & pharmacovigilance un regulatory...

The metabolics medical advisor will report to the medical affairs manager, metabolics... educate the  medical community with up-to-date medical and scientific...

Clear understanding of medical affairs compliance requirements... practical knowledge of clinician-facing medical affairs functions... ability to effectively collaborate...

The global development medical director plays a critical role in the medical monitoring of a clinical study ensuring safety to patients... clinical input to (s)nda/(s)bla)...

The senior global development medical director plays a critical role in the medical monitoring of a clinical study ensuring safety to patients...

The clinical research medical advisor is a global clinical development role with medical responsibility for the clinical trial process...

Summary clinical research medical advisor - haemato-oncology, spain, #li-remote... the clinical research medical advisor is a global clinical development role with...

• collaborate efficiently on clinical safety tasks with colleagues from clinical development, regulatory affairs, medical affairs, medical information, statistics...

• moderate understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting • good problem-solving and critical...

Specialized focus on digital regulatory science, clinical medical affairs, pv (pharmacovigilance), sustainability, and other science-related project activities...

Drug supply, contracting, regulatory documentation, publication review etc... the edd will work hand in hand with the scientific study leader who is responsible...

Possesses general knowledge of 1) medical monitoring 2) regulatory approval process in relevant countries; 3) pharmaceutical industry/r&d operations; 4) marketing...