Specialist in pharmacovigilance in BIOSAYNS UKRAINA, OOO

The company BIOSCIENCES UKRAINE LLP is one of the leaders in providing full-cycle consulting services registration procedures, marketing, logistics and pharmacovigilance. The reliability and stability of the company has been proven by time, and the quality and efficiency is achieved by the coordinated work of a team of real professionals.

In connection with the expansion of the staff, the company < b style="font-weight: 700">Bioscience Ukraine announces recruitment for the position of Professional of the Pharmacovigilance Department.

Requirements:

• Higher medical or pharmaceutical education (priority for a candidate with a medical education);
• Experience in the field of pharmacovigilance from the 1st year;
• Knowledge of the regulatory legislation of Ukraine, that regulates pharmacovigilance activities and the Guidelines and Directives of the European Union and the Eurasian Economic Union (GVP);
• Experience of working with instructions for the medical use of medicinal products (preferred);
• Knowledge of Ukrainian and European legislative framework in the field of pharmacovigilance and registration (preferred);
• Ability to work with the standard Microsoft Office package, The level of English is not lower than Intermediate.
• Personal qualities: proactivity, analytical mindset, politeness, responsibility, attentiveness, desire for professional development, ability to work in a team and in multitasking mode;

Responsibilities:

• Reception of information on adverse reactions and/or lack of effectiveness of drugs, analysis, communication with the source of the message, collection of follow-up, transmission to the SEP;
• Maintenance of the quality system in to the pharmacovigilance system (in particular, updating SOPs;
• Revision and updating of the IFSF;
• Monitoring of safety information on the websites of local and international regulatory bodies;
• Preparation of materials and training on pharmacovigilance (for marketing, distribution, etc.);
• Development of regularly updated safety reports (ROSB/ PSUR);
• Development of risk management plans (RMP/RMP);
• Working with the system database pharmacovigilance;
• Supporting the procedures of registration, re-registration of medicinal products according to various types of procedures in accordance with legislation (development of instructions for medical use, PURs, DKO/ADCO, Summary of safety data).

Terms of use:

• Work in a stable company
• Official employment and social guarantees according to the Labor Code
• Decent salary level
• Medical insurance
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• Opportunities for professional growth
• Democratic and loyal management
• Comfortable office near the Poshtova ploshcha metro station
• Tea, coffee, sweets

Please send your CV for considerationin

We will be glad to see you in our team!

In your resume, please add a photo and indicate the desired salary level.

Natalia, phone.067-509-01-40