Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Drug Safety Logistics Associate (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Projektbeschreibung
REFERENZNUMMER:
375025/11
IHRE AUFGABEN:
-Tracking and distribution of adverse event reports associated with investigational and marketed products for booking adverse events in the safety database
-Maintaining internal record systems and providing status reports as required
-Sorting, collecting, and assembling safety relevant information received in Drug Safety
-Booking cases in Argus Safety for investigational and marketed products, and assessing them according to urgency
-Reviewing submission requirements and planning activities in order to meet deadlines
-Overseeing and assisting in the preparation, compilation, dispatch, tracking and follow-up of submissions
-Troubleshooting and proactively following-up on any issues that arise pre- or post-submission
IHRE QUALIFIKATIONEN:
-Bachelor’s degree or equivalent education
-Experience in the pharmaceutical or biotechnical industry is an advantage
-Understanding of SUSAR-related safety submissions or knowledge of medical terminology
-Computer proficiency and knowledge of safety databases
-Ability to communicate effectively in English, French or German are helpful
-Ability to prioritize tasks and ability to work under pressure in order to meet tight timelines
WEITERE QUALIFIKATIONEN:
Drug safety assistant
375025/11
IHRE AUFGABEN:
-Tracking and distribution of adverse event reports associated with investigational and marketed products for booking adverse events in the safety database
-Maintaining internal record systems and providing status reports as required
-Sorting, collecting, and assembling safety relevant information received in Drug Safety
-Booking cases in Argus Safety for investigational and marketed products, and assessing them according to urgency
-Reviewing submission requirements and planning activities in order to meet deadlines
-Overseeing and assisting in the preparation, compilation, dispatch, tracking and follow-up of submissions
-Troubleshooting and proactively following-up on any issues that arise pre- or post-submission
IHRE QUALIFIKATIONEN:
-Bachelor’s degree or equivalent education
-Experience in the pharmaceutical or biotechnical industry is an advantage
-Understanding of SUSAR-related safety submissions or knowledge of medical terminology
-Computer proficiency and knowledge of safety databases
-Ability to communicate effectively in English, French or German are helpful
-Ability to prioritize tasks and ability to work under pressure in order to meet tight timelines
WEITERE QUALIFIKATIONEN:
Drug safety assistant
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Sonstiges