Description
Drug Safety Logistics Associate (m/f)
Reference: -en
Start: ASAP
Duration: 12 MM+
Main tasks:
- 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
Main qualifications
- 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
Main advantages:
- A highly motivated team and an open way of communication
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.