Pharmacovigilance Specialist

Company: Нигина Исмаилова

Tashkent

Salary: 5000000 – 8000000 UZS

Pharmacovigilance Specialist at OOO Astor Alliance (No experience required) Salary: 5,000,000 - 8,000,000 UZS with KPI Work Format: On-site Work Schedule: 6/1, 9:00 AM - 6:00 PM Address: Tashkent, 1a Ipakchi str. Description The main goal of the role is to collect, register, and analyze information on adverse drug reactions under the guidance of an experienced specialist. Responsibilities: Monitoring and collecting spontaneous reports of adverse drug reactions. Processing and evaluating incoming reports of adverse reactions. Maintaining a database of adverse reactions. Preparing drug safety reports for regulatory authorities. Interacting with medical professionals and patients on adverse reaction matters. Participating in the development and updating of drug instructions regarding safety. Assessing safety signals and conducting risk analysis. Requirements: Experience in the pharmaceutical industry; Work experience of 1-3 years; ​​​​​​​ Higher pharmaceutical or medical education; Knowledge of Russian, Uzbek, and English (preferred) languages; Desire for growth and development; Communication skills and responsibility. Your Benefits: What we offer you: A comfortable office at the address: Almazar district, Karakamysh 2/3 Work in a stable, growing company with a sought-after product! Company-sponsored training and mentorship; Employment according to the Labor Code of the Republic of Uzbekistan (A civil contract is concluded for the probation period), probation period of 2 months; Lunch on company premises; Reimbursement of travel expenses (for work-related matters); Corporate mobile communication; Official salary credited to card without delays; Annual leave (21 calendar days). Work schedule 6/1 from 9:00 AM to 6:00 PM (Saturday is a short day from 9:00 AM to 1:00 PM) Required Skills: Preparation of pharmacovigilance reports (PSUR, PBRER, DSUR) Collection, evaluation, and registration of adverse event reports Monitoring scientific literature on drug safety Knowledge of regulatory requirements and pharmacovigilance guidelines (ICH, CIOMS, local) Participation in the development and update of Risk Management Plans (RMP) Working with drug safety databases (Argus, ARISg) Processing medical inquiries related to drug safety Preparation for pharmacovigilance audits and inspections

Responsibilities

• Monitoring and collecting spontaneous reports of adverse drug reactions.
• Processing and evaluating incoming reports of adverse reactions.
• Maintaining a database of adverse reactions.
• Preparing drug safety reports for regulatory authorities.
• Interacting with medical professionals and patients on adverse reaction matters.
• Participating in the development and updating of drug instructions regarding safety.
• Assessing safety signals and conducting risk analysis.

Requirements

• Experience in the pharmaceutical industry;
• Work experience of 1-3 years;
• ​​​​​​​ Higher pharmaceutical or medical education;
• Knowledge of Russian, Uzbek, and English (preferred) languages;
• Desire for growth and development;
• Communication skills and responsibility.

Benefits

• What we offer you:
• A comfortable office at the address: Almazar district, Karakamysh 2/3
• Work in a stable, growing company with a sought-after product!
• Company-sponsored training and mentorship;
• Employment according to the Labor Code of the Republic of Uzbekistan (A civil contract is concluded for the probation period), probation period of 2 months;
• Lunch on company premises;
• Reimbursement of travel expenses (for work-related matters);
• Corporate mobile communication;
• Official salary credited to card without delays;
• Annual leave (21 calendar days).
• Work schedule 6/1 from 9:00 AM to 6:00 PM (Saturday is a short day from 9:00 AM to 1:00 PM)

Skills

• Preparation of pharmacovigilance reports (PSUR, PBRER, DSUR)
• Collection, evaluation, and registration of adverse event reports
• Monitoring scientific literature on drug safety
• Knowledge of regulatory requirements and pharmacovigilance guidelines (ICH, CIOMS, local)
• Participation in the development and update of Risk Management Plans (RMP)
• Working with drug safety databases (Argus, ARISg)
• Processing medical inquiries related to drug safety
• Preparation for pharmacovigilance audits and inspections