Pharmacovigilance Specialist - 6081 (m/f)

REFERENZNUMMER:

367044/11

IHRE AUFGABEN:

-Responsible for 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
-Responsible for the reconciliation of adverse events reports received from other MSD operating units (e.g., Designated Point of Contact, Medical Information, etc.) and contractual partners, as applicable
-Responsible for the filing, storage and archiving of 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

IHRE QUALIFIKATIONEN:

-University degree in Life Sciences, Medical Science or another relevant discipline
-Good understanding of Pharmacovigilance regulations in Switzerland as well as pharmacovigilance practices and standards; awareness of Pharmacovigilance systems
-Previous experience in the pharmaceutical industry
-Strong project management skills with the ability to prioritize assignments; excellent time management, organizational and planning skills
-Proficiency in Good Documentation Practices and awareness of Good Clinical Practice concepts
-Familiarity with the use of a safety databases and demonstrated ability to learn new computer interface systems
-Excellent communication skills in German and English, both verbally and in writing. Additional skills in French would be a plus

WEITERE QUALIFIKATIONEN:

Drug safety assistant