TRABAJO REGULATORY AFFAIRS ASSOCIATE STUDY BARCELONA, BARCELONA

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

Organizes regulatory information, logs and tracking... maintains regulatory files/database and chronologies in good order... participate in the product development...

Managing and maintaining comprehensive and accurate records of regulatory submissions, approvals, and correspondence providing guidance and support to study teams...

Excellent understanding of clinical study management including monitoring, study drug handling and data management... experience in all study phases and in rare...

Represent the clinical study team at the clinical sub team... liaising with other functions to design external expert consultations, contribute to the development...

You will work closely with study implementation teams, as well as clinical operations, data management and regulatory affairs to ensure the solutions meet the requirements...

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

• collaborate with key stakeholders, including medical affairs and other partner functions... the associate director, medical communications & information, is accountable...

Prepare and present findings from real-world evidence studies to internal and external stakeholders, including scientific conferences, ministries of health, regulatory...

Administer protocol and related study training to assigned sites and establish regular lines of communication... as an experienced clinical research associate, you...

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...