TRABAJO GLOBAL REGULATORY AFFAIRS ASSOCIATE BARCELONA, BARCELONA

Position: regulatory affairs management director (rad), regulatory science & execution, global regulatory affairs location: barcelona - spain (3 days working from...

Experience in regulatory affairs business processes is a plus (e... we are looking for an experienced individual in global drug development regulatory affairs to...

With our expertise, we interpret, anticipate, and shape global health authority expectations to build insightful cmc and device regulatory strategies...

Accountabilities • support global study director (gsd) / global study associate director (gsad) and global study managers (gsms) by completing delegated study...

Coordinate and prepare regulatory documentation, including technical files, for submission to global regulatory authorities... at least 2 years of experience in...

Organizational skills in planning, strategizing, managing, and monitoring regulatory changes... you will keep updated on the regulatory environment in the region...

Proven project management experience on a global level... the global study associate director (gsad) is responsible for the delivery of clinical studies, including...

Work closely with regulatory to develop effective regulatory and cmc strategies... responsibility is shared across global and local markets...

Para alcanzar nuestro propósito y con el objetivo de aportar valor significativo y diferencial a las personas que sufren dolencias graves, en ferrer hemos definido...

Viders and regulatory bodies astrazeneca embraces diversity and equality of opportunity... we welcome and consider applications to join our team from all qualified...

Establish a global mindset to systematically gather, consolidate & communicate regulatory authority and industry intelligence for the proactive continuous improvement...

Lead and contribute to medical monitoring of trials provide expert medical input into the preparation of regulatory documents and interactions with regulatory authorities...

Strong understanding of regulatory requirements and guidelines for clinical trials, including ich-gcp and local regulatory requirements... in addition to your competitive...

Your ability to work collaboratively will facilitate cross-functional interactions with colleagues from across astrazeneca and externally, including counterparts...

Oversee regulatory risk, change management, and assurance activities, including sample auditing and feedback/escalation on compliance...

As global market development project manager - rhinology & gastroenterology vie in our global dupixent team, you’ll participate in the implementation of market...

This is what you will do: the associate director, biostatistics has sufficient experience working as a statistician in the pharmaceutical industry to independently...

For associate director role, experience of program design knowledge of the technical and regulatory requirements related to the role leadership capabilities to be...