Beschreibung
Drug Safety Logistics Associate (m/f)
Reference: -en
Start: 05/19
Duration: 12 MM++
Main tasks:
- Responsible for coordinating the tracking and distribution of adverse event reports associated with investigational and marketed products
- Booking adverse events in the safety database
- Maintaining internal record systems
- Providing status reports as required
- Manage the logistics for submissions made by the GDS Submissions Group
Main qualifications
- Bachelor’s degree or equivalent education
- Experience in the pharmaceutical or biotechnical industry, training in a health related field
- Understanding of SUSAR-related safety submissions or knowledge of medical terminology and familiarity with disease processes is a plus
- Computer proficiency (Word, Excel and PowerPoint), knowledge of safety databases or the ability to learn new systems
- Ability to communicate effectively in English (spoken and in writing) French and/or German are helpful
- Attention to detail
- Ability to prioritize tasks
- Ability to work independently on routine tasks
- Good organizational and problem solving skills
- Ability to work under pressure and to meet tight timelines
Main advantages:
- A very renowned company
- Pleasant working atmosphere
- You will work in an international and team-oriented environment
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.
My contact at Hays:
My contact person:
Dominic Yves Peter
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