About
Summary
Currently seeking a chance to work in a creative and collaborative environment, where my analytical skills, Pharmacovigilance/Drug Safety and Academic Knowledge will contribute to the overall goal of the organization while further developing my leadership, organizational and technical skills.
Positions
Pharmacovigilance and Scientific Officer Jan 2017 - Oct 2017
To elaborate the documents regarding pharmacovigilance in accordance with the law , to
collect, to process and to submit data to the EU QPPV with a copy to the responsible
persons from MLD Tradiing EOOD Bulgaria
To update the documents according to the national and european legislation
To elaborate/review Standard Procedures for pharmacovigilance and to be Local
Pharmacovigilance Responsible Person in Romania when needed
To prepare documents for audit and for standard procedure dossiers
To make a periodic training for the medical representatives
To elaborate data bases, to monitor adverse reactions for the products in the portfolio or
similar products (from literature)
To monitor new legislative changes and to communicate to the EU QPPV with a copy to
the responsible person from MLD Trading EOOD Bulgaria
To manage literature data and referance data bases
To introduce new adverse reaction in the data bases
To update electronic data base with daily new information about adverse events
To report promptly any adverse reaction of company’s medicines to the EU QPPV with a
copy to the responsible persons from MLD Trading EOOD Bulgaria
Follow up SAE/SUSAR
Maintaining liaison with operational managers involved in clinical trials
Education
University Politehnica of Bucharest 2011 - 2015
Field of study: Chemistry
Degree: PhD
PhD doctoral thesis : „Functionalization of multi-walled carbon nanotubes for medical applications"
▪ I established a new method of administration of cancer drugs
▪ I realized technical and scientific documentation
▪ I work methods validated according to data specialist ( according to FRX, GMP, GCP and literature)
▪ I attended conferences and meetings with mixed teams of both national and international research▪ I
gave support and specialized working groups
Skills
▪ High level of integrity and ethics
▪ Good knowledge of Pharmacology
▪ Strong attention to detail
▪Proven flexibility and adaptability
▪ A real team player
▪ Ability to extract pertinent information from all study documents
Good organizational skills gained as research.
CV
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