The role profile is described as follows:
Main accountabilities:
Records, screens and categorises reports of adverse drug reactions in clinical studies
Coordinates tracking and evaluation of adverse drug reaction reports
Compiles and submits reports on cases of suspected adverse drug reactions to authorities
Updates standard safety information documents and procedures
Participates in international safety forums/meetings
Reports adverse events to internal sources and external regulatory authorities
Maintains and uses Amgen International Database and other relevant data collection tools
Collects and provides follow-through resulting in timely and accurate to reporting and archiving
Collects, analyses and communicates information regarding safety profiles for developing/marketed
products
Screens local literature for expediting safety reports

The ideal candidate would possess:
Minimum Requirements
Degree in scientific area
3 or more years of related industry experience
Fluency in local language and English, both in oral and written communication

Preferred Requirements
Knowledge of information management and database administration
Prior experience in training
Amgen Hellas offers a highly competitive remuneration package,
as well as excellent career opportunities.

To apply, please visit our career center at: www.amgen.com/careers
and apply for the position of
“Senior Associate Global Safety Job code: 367BR “