Senior Specialist, Pharmacovigilance
Responsibilities:
- Screening scientific literature by using the internal search mechanism and/or by making use of external tools and providers.
- Classification of references of safety-relevant publications.
- To keep track of the internal literature ordering process.
- Data entry of literature reports into the safety database.
- Preparation of standard reporting forms (e.g., CIOMS I / MedWatch Forms and XML .
- Case completion / documentation.
- Downloading, reviewing and sharing of client specific ICSRs from MLM service of EMA.
- Performing duplicate search of literature cases against updated information in Medical Literature Monitoring (MLM) service provided by EMA.
- Act as main contact for client/project management.
- The employee agrees to take over primary listed tasks and responsibilities in other service lines and additional reasonable tasks that align with their abilities, qualification and training, if required.
- Professional education or University degree in Life Science.
- Basic understanding/knowledge in the field of pharmacovigilance.
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Education:
- University degree in Life Science
Work Experience:
- Two years experience and knowledge in the field of pharmacovigilance
Skills:
- Communication & presentation skills: Good communication skills (written and verbally)
- Good presentation skills
