Currently we are looking for Jr. Pharmacovigilance Specialist located in Moscow for the period of replacement of the employee on maternity leave.

Major Accountabilities:

• Process spontaneous and solicited / clinical trial adverse events reports (includes receipt, assessment of seriousness/labeling, prioritization and requesting follow-up, case closure and archiving) and enter them into the Global Safety database;
• Request appropriate follow-up information;
• Submit spontaneous and solicited / clinical trial individual case safety reports to the Local Health Authority;
• Process all cases within specified timelines;
• File, store and archive safety-related data;
• Assist in preparation for PV audits/inspections;
• Assist in delivery of PV training;
• Perform other activities as requested by the Pharmacovigilance Country Lead.

Requirements to the candidate:

• Higher Education - Medical or pharmaceutical is preferable;
• Experience of working in Pharmaceutical company from 1 year;
• English - Upper-intermediate level required;
• Ability to learn safety databases;
• Strong time management and organization skills;
• Strong communication skills and relates well to all kinds of people;
• Ability to work independently with minimal supervision;
• Accuracy in details.