Employee Information
Full Name:
Born:
Education:
Brankica Moskova
Specialist for Pharmacy Regulatory Affairs and Pharmacovigilance
Job Title:
QC analyst
Business Title:
Pharmacovigilance assosiate
Country of Residence:
Republic of North Macedonia
Email : ********.***********@*****.***
Phone number: +389********
Summary
.
Brankica Moskova has over 16 years of experience in pharmaceutical industry with a strong background in Drug Efficacy and Drug Safety.
From June 2004, till February 2006 Brankica is a member of F&M Medical Device team as Regulatory Affairs Assistant in Bitola.
From March 2006 she joined Mak-Lek Jaka 80 Pharmaceutical team as a chief Pharmacist in Retail Pharmacy in Prilep.
From July 2010, as a member of Zegin-Pharm team, Brankica is involved in Marketing, Retail Pharmacy and Drug Efficacy in Prilep.
Since January 2018, as a member of Bulgarian and Balkan team at Social Data Monitoring Project by IQVIA, Brankica is involved in pharmacovigilance data review in various therapy areas.
Brankica worked as a PV analyst until September 2018 and became QC analyst for Balkan and Bulgarian languages, and now she is still working as QC analyst updated for Spanish, French and Italian country.
Formal Educational History
Last Date Attended
Institution Name, Country
Education Level/Degree
Area of Study
Completion Status
31.05.2002
Faculty of Pharmacy –
Master of Pharmacy
University” Ss’ Cyril & Methodius”, Skopje – N.Macedonia
Master of Pharmacy
Pharmacy
Graduated
10.05.2018
Specialization for Regulatory affairs and Pharmacovigilance Faculty of Pharmacy in University “Ss Cyril & Methodius” Skopje- Macedonia
Postgraduate
Specialist for Pharmacy Regulatory Affairs
Pharmaceutical Regulatory Affairs
Major subject- Pharmacovigilance
Graduated
Employment History
IQVIA Employment History
Date of Employment:
01/2018- contract by Verticl.xyz - still
Job Title:
QC analyst - remote
Business Title:
Drug Safety
Key Responsibilities:
Responsibility to recognize and report Adverse Events, Customer Feedback and Product Quality Copmlaint as well as all Informations about
the safety, quality and performance of drug
PV analyst – Analyze,identify and report adverse events from patient data from Social Media sites across various therapy areas/brands by applying analytical and logical reasoning while adhering to client specific guidelines
QC analyst – Monitoring PV’s reviewed records about adverse events. Weekly attends meetings and training and ensures 100% accuracy by conforming to the SOP’s.
Non-IQVIA Employment History
Date of Employment:
06/2004 – 02/2006
Name of Employer:
F & M Medica
Job Title:
Regulatory Affairs Assistant
Key Responsibilities:
studying scientific and legal documents, gathering, evaluating, organising, managing and collating information in a variety of formats, ensuring compliance with regulations set by the Medicines and Healthcare products Regulatory Agency maintaining familiarity with company product ranges.
Date of Employment:
03/2006-07/2010
Name of Employer:
Mak-Lek Jaka 80
Job Title:
Chief Pharmacist
Key Responsibilities:
Chief pharmacist
Managing the work flow in the drug store, supply medicine and orthopedic products, work with all healthcare representatives and healthcare insurance.
Controls medications by monitoring drug therapies; advising interventions.
Completes pharmacy operational requirements by organizing and directing technicians' work flow; verifying their preparation and labeling of pharmaceuticals; verifying order entries, charges, and inspections.
Select, give advice on and supply non-prescription medicine, sickroom supplies and other products.
Date of Employment:
07/2010-01/2018
Name of Employer:
Zegin-Pharm
Job Title:
Retail Manager
Key Responsibilities:
Retail Pharmacist and Store Manager
Ensuring the highest professional standards of counter prescribing
Medicines Protocol implementation
Management and control of medicine supply of the unit
Planning, supervision, and coordination of all activities related to the pharmacy’s operations
Ensuring that staff training and staff knowledge is kept up to date in order
to deliver peak performance
Establishing effective teamwork
Establishing positive relationships with customers, pharmaceutical
representatives/manufacturers, medical professionals, healthcare
organizations and insurance providers.
Resolving customer complaints
Management and control of supplies
Providing financial analyses of sale
Resolving customer complaints and control of supplies
Department Specific Experience
Department: Lifecycle Safety
Category
Experience
PV analyst – Analyze,identify and report adverse events from patient data from Social Media sites across various therapy areas/brands by applying analytical and logical reasoning while adhering to client specific guidelines.
8 months as PV
QC analyst – Monitoring PV’s reviewed records about adverse events. Weekly attends meetings and training and ensures 100% accuracy by conforming to the SOP’s.
2 years and 1 month as QC
Language(s)
Language
Speaking
Reading
Writing
Macedonian
Native
Native
Native
Bosnian
Native
Native
Native
Serbian
Native
Native
Native
Croatian
Native
Native
Native
Bulgarian
Fluent
Fluent
Fluent
English
Fluent
Fluent
Fluent
Current Memberships in Professional Organizations
Macedonian Pharmaceutical Chamber
Macedonian Pharmaceutical Society
Other Relevant Information
Licenses and Certifications
Active Licence for Pharmaceutical Practise in the Republic of Macedonia
09.January 2018- Certificate of Completion – Know to Report – Adverse Experiences & Product Quality Complaints v3.1
June 2018 Certificate in Current Pharmacovigilance Regulatory Landscape