18 ago - Roma
Abbvie
**Company Description**
**Job Description** Key Responsibilities**: - Responsible of collecting recording, processing, conducting follow up, translating and filing of adverse events (AE) and other safety information reportable to PPS from spontaneous and solicited sources according to local and international requirements, in accordance to applicable SOP/Guideline
- In collaboration with pharmacovigilance team, as per assigned local literature articles, conduct the review, as detailed in the Global SOP.
- In collaboration with pharmacovigilance team, conduct local QC, as detailed in the Global SOP.
- Ensure reconciliation of cases as per Global procedure
- Support pharmacovigilance team in ensuring compliance of affiliate PV quality system.
- Support pharmacovigilance team in ensuring Organized Data Collection Programs are conducted in compliance of PV requirements.
- Support pharmacovigilance team in affiliate and third partner company staff pharmacovigilance training administration as per applicable procedures.
- Support pharmacovigilance team in aggregate safety reporting activities.
- To undergo training relevant to the function and to be familiar and updated with the AbbVie local and international procedures relevant to the Job Description **Qualifications** Requirements**: - Medical, pharmacy, biology, biotechnology or related degree
- Fluency in written and oral English is essential in order to facilitate communications with global team (B2/C1 level)
- Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity
- Ability to translate strategy into feasible and realistic medical actions
- Good knowledge of the health sector and its development
- Capability of working effectively in a matrix structure
- Ability to get things done and demonstrated strong sense of urgency. **Additional Information** US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
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