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Pharmacovigilance Executive Resume Sample, Experience : 3 years

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Name of the Candidate:[Private]
Name of the Post Applied:Pharmacovigilance Executive
Job related skills / software:safety processing expert, Argus 7
Sub Category:Pharmacovigilance
Years of Experience:3 years
Salary Expected per Month(Rs):30,000 to 40,000
Highest Qualification attained:M.Sc. / MSC : Master of Science
Major / Specialization:Pharmacovigilance
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 :


Vidyasagar S Morkhandikar
M.Sc. (Pharmaceutical Medicine)
Contact No. – 91 9920631447
E-mail Address – sagar.morkhandikar AT gmail.com
Current Address- C-B, Flat No 604, Pariwar society, Kanjur Marg (E), Mumbai 400042.

Career Objective  :
To work in a strong, forward thinking, progressive and equal opportunity organization where I can apply the knowledge I have obtained, involving maximum utilization of my skills and experience to deliver beyond expectations so as to produce growth oriented results.

Current Employer  :
Cognizant Technology Solutions (Airoli, Navi Mumbai)
Designation  : Junior Data Analyst (Case Processing Associate) in Pharmacovigilance department
Current CTC  : 2.93 Lac per annum
Duration  : From 09 Apr 2012 to Present(1 year 10 months)

Roles and Responsibilities  :
Hands on experience of ARGUS 7.0 database
Review of source documentsincluding physician’s medical records/pharmacy records/complaints received from marketing programs etc.
Triaging ofcases based on their seriousness and validity.
Data Entryof the adverse events report (AE) form from source docs including patients demographical data, suspect and concomitants, narrative, selection and detailing of adverse events, action taken, dechallenge and rechallenge, medical history and diagnostic details.
Codingof Suspect and Concomitant drugs using Company and WHO-DRUG dictionaries.
Coding of verbatim termsusing MedDRA for patient history, investigations, product indication and event term.
Seriousness determination and Causality assessment.
Listedness assessmentof adverse events (AE) using various labelling documents.
Meeting the timelines and supporting global regulatory submissions in expedited reporting of ICSRs.
Delivering the ICSR on various case types including Spontaneous, PMS study, Compassionate use cases, Literature study, and Discharge summary.
Quality Review of non-serious cases.
Member of Query chasingand Query Resolution Team.
Allocation of casesas per seriousness and regulatory timelines.
To train and mentoringthe new employees.
Co-ordinate with Team Lead, Quality Reviewer, Medical Reviewer and Team Manager to ensure efficient case processing.

Past Working Experience  :
01 year(from Aug 2009 to Jul 2010) experience in Phase III clinical trial as a site co-ordinator trainee in Clinsearch Healthcare Solutions Pvt.

Ltd. Thane (West).

Academic Credentials  :
M.Sc. Pharmaceutical Medicine K.E. M hospital and Seth G.S medical college, Mumbai (MUHS, Nashik) 2013 56.60%
B. Pharm Maharashtra college of pharmacy, Nilanga (SRTMU, Nanded) 2009 64.50%

Certification  :
Certificate course on Basics of Intellectual Property Rights (DL-101) from WIPO Geneva.

Strong interests to know more about new technologies.
Excellent process oriented team player with a good learning curve.
Ability to work harmoniously with a broad spectrum of people.
Attention to detail
Concern for quality

Hobbies and Interests  : Playing Cricket, Listening music, Travelling etc.

Languages Known  : English, Hindi and Marathi.

Personal Details  :
Gender - Male
Date of Birth -24 Apr 1987
Marital Status - Single
Permanent Address-Shivkrupa colony, Old Ausa Road,
Behind Datta Mandir,
Latur, Maharashtra-413521

Declaration  :
I hereby declare that all the information mentioned above is true to the best of my knowledge.

Yours Sincerely,
Vidyasagar S Morkhandikar


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