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Drug Safety Associate Resume Sample, Experience : 2 years

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Name of the Candidate:[Private]
Name of the Post Applied:Drug Safety Associate
Job related skills / software:Comprehensive knowledge of international drug safety and pharmacovigilance principles and regulations, Extensive knowledge of drug safety and drug development process and procedures, In-depth knowledge of coding principles, submission criteria, regulatory timeline requirements, technical requirements and guidelines.
Category:Medical
Sub Category:Drug Safety Physician
Years of Experience:2 years
State:Telangana
Gender:Female
Salary Expected per Month(Rs):15,000 to 20,000
Highest Qualification attained:B.Pharm. : Bachelor of Pharmacy
Major / Specialization:Industrial Pharmacy
Email Id:[Private]
 
Are you looking for job now?:Yes
Can the recruiter contact you?:Yes
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Resume Format / CV Sample Template / Example / Model :

    

Alice Augustina
watkins.wonderland AT gmail.com
Plot.no-32, Door.no-F1,
Sai Krupa Officers Colony,
Yapral, Secunderabad – 87,

Career Objective :
To secure a position with a reputable company in which I can exercise my knowledge gained during my professional experience.

Professional Experience :
Worked as an Associate at Cognizant Technologies for a period of 21 months i.e., from Oct 28 2013 –May 28 2015.
US insurance healthcare process “Anthem” also known as “Wellpoint”.

Job role :
Claims Pre-adjudication :
** In this role I review medical records of the insurer of 5central and 3 western states of America.
** The pre-adjudication system increases profitability by identifying avoidable denials and recommends
** Solutions before claims are submitted to payers.

Tools Experience :
WGS : utilized this tool to acquire provider details and treatment dates.
Blue Square : utilized this tool to review medical record.
BPM : BPM template to send letters to provider.
WCF : utilized to review claim form.
GPOO : utilized this tool to search for a provider region.

Core competencies :
** Comprehensive knowledge of international drug safety and pharmacovigilance principles and regulations.
** Extensive knowledge of drug safety and drug development process and procedures.
** In-depth knowledge of coding principles, submission criteria, regulatory timeline requirements, technical requirements and guidelines.
** Possess sound communication skills, both in verbal, and written.
** Familiar with basic comp


uter and database applications.
** Good leadership, analytical, problem solving and time management skills.

Professional Pharmacovigilance Training at Excel Lifetech :
** Handle responsibilities of reviewing and processing adverse events reported by investigators.
** Perform the tasks of conducting research and analyzing medical and scientific literature.
** Responsible for providing medical and scientific information to health care professionals.
** Perform the tasks of reviewing bioequivalence study protocols, clinical trial protocols, and provide support the clinical trial team.
** Handle responsibilities of developing concise, accurate, and well-written case narratives.
** Perform the tasks of maintaining the safety database and perform coding of diseases as well as adverse events according to the project-specific coding conventions (MedDRA and WHODD).

Technical Skills :
ARGUSSafety Database ORACLE Health Sciences

Education :
P.G Diploma In Pharmacovigilance : Excel Pharma
Bachelor of Pharmaceutical Sciences 2013 from T.V.M college of Pharmacy (Bellary) affiliated to Rajiv Gandhi University of Health Sciences, Bangalore, KA.
Intermediate Sri Chaitanya Junior Kalasala Ecil 2005.
Secondary School of Education : Valerian Grammar School Bolarum 2003.

Key strengths :
** Ability to work in a team.
** Determination towards work.
** Positive attitude towards life
** Capacity to deal with stress.

Personal Profile :
Date of birth : 22/09/1987.
Hobbies : watching TV and reading books.
Languages Known : English, Telugu, and Hindi.

The above information is true to the best of my knowledge.

Alice Augustina.

Date : 09/11/2015
 

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