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 : adhzwp@r.postjobfree.com

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

Contact this candidate