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Pharmacovigilance Specialist

Job Field:
Regulatory and Drug Safety Jobs
Discipline:
Pharmacovigilance Jobs
Country:
Switzerland
Region:
Switzerland All
Contract Type:
Permanent
Currency:
Unspecified
Salary Description:
Competitive
Posted:
30-Apr-18
Recruiter:
Clintec
Job Ref:
SWI-PVSPEC-6081

Pharmacovigilance Specialist – Lucerne, Switzerland

Clintec is actively recruiting a Pharmacovigilance Specialist to join our expanding company in Switzerland. This is a full-time and office-based role working assigned to one of our global pharmaceutical clients based in Lucerne.

Role Description

The Pharmacovigilance Specialist will be responsible for the day-to-day management of all pharmacovigilance activities in Switzerland, ensuring compliance with PV processes/regulations, corporate policies/procedures and monitoring of adverse events. The Pharmacovigilance Specialist will report to the Pharmacovigilance Country Lead.

Responsibilities of the Pharmacovigilance Specialist:

Day-to-day adverse experience case management including case intake and follow-up activities, the review of local and health authority submissions of cases
Responsible for aggregate safety report submissions
Reconcile of adverse events reports received from other internal company operating units (e.g., Designated Point of Contact, Medical Information, etc.) and contractual partners, as applicable
File, store and archive safety-related data
Assist in preparation for audits/inspections for their country/territories and may participate in the audit and/or inspection
Assist in the delivery of training to PV staff and customer facing non-PV staff (e.g., Sales Reps, Medical Information, etc.) and distributors/vendors/business partners

Essential Criteria:

Bachelor’s Degree (or equivalent) in a Life Science, Medical Science or relevant discipline
Previous experience working within the pharmaceutical/clinical research industry
Sound understanding of pharmacovigilance regulations in Switzerland
Strong project management skills with the ability to prioritize assignments/manage time
Good Documentation Practices and awareness of Good Clinical Practice concepts
Compliance mindset/focused, high level of accuracy and quality in work
Familiarity with the use of a safety databases and demonstrated ability to learn new computer interface systems
Strong collaboration skills with the ability to work across different departments
Proven ability to work independently with minimal supervision
Excellent communication skills in German and English, both verbally and in writing - Additional skills in French would be a plus

Closing Date:
04/05/2018

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