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Medical Writer Resume Sample, Experience : 6 years

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Name of the Candidate:[Private]
Name of the Post Applied:Medical Writer
Job related skills / software:Medical writing (Domain ),Clinical data management.,& Drug Safety( PV )-core, quality check on the clinical study, periodic adverse drug experience , case processing, safety narrative and adverse events of pfizer drugs international received from clinical research organization and international market/drug safety ( spontaneous, periodic ,pms)
Category:Medical
Sub Category:Clinical Research
Years of Experience:6 years
State:Maharashtra
Gender:Male
Salary Expected per Month(Rs):50,000 to 60,000
Highest Qualification attained:M.Pharm. : Master of Pharmacy
Major / Specialization:Medicinal
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 :

    

Curriculum Vitae :
Mr.Varinder Singh

Career Objective :
I am an industry savvy pharma professional for the most reputed brand in pharma market (corex and becosules). After gaining hands-on experience . I am looking forward to work with an organization that will enhance my potential and help utilize my professional expertise to achieve excellence in professional world through my skills, hard work and sincere efforts and to prove as valuable asset for my organization.

Academic qualification :
** M. PHARM (MEDICINAL).1st CLASS-2003
** PASSED BACHELORS IN PHARMACY FROM NAGPUR UNIVERSITY, NAGPUR 1ST CLASS YEAR 2001
** PASSED DIPLOMA IN PHARMACY PANAJI GOA YEAR 1996.
** PASSED HIGHER SECONDARY EXAMINATION (CBSE BOARD) FROM GOA (PCB 74%)
** PASSED MATRICULATION EXAMINATION (CBSE BOARD) FROM GOA
** PURSUING POST GRADUATE DIPLOMA IN CLINICAL RESEARCH,CLINICAL-
** DATA MANAGEMENT,SAS AND MEDICAL WRITING FROM CLINIMINDS-MUMBAI

Experience :
Worked with Pfizer India as PSO (PROFFESIONAL SERVICE OFFICER
Worked with reliance as SUPPORT ASSOCIATE-OPERATIONS March 2012-jan2014
Worked with COGNIZANT TECHNOLOGY SOLUTION Safety data manager (pharmacovigilance ) & clinical Data Management Feb 2006-mar- 2012.

Job profile  :
Pharmacovigilance :
1) Medical writing( Domain ),Clinical data management.,& Drug Safety( PV )-core, quality check on the clinical study, periodic adverse drug experience , case processing, safety narrative and adverse events of pfizer drugs international received from clinical research organization and international market/drug safety ( spontaneous, periodic ,pms
** To answer technical queries related to the pfizer product intenationaly like lipitor ,norvasc,viagra etc.
** Trained on different sop’s related to products like lipitor ,viagra,Devices etc
** Safety reporting, tracking and review (ARISG), oracle AERS –tracking GLOBAL SAFETY DATA MANAGEMENT PROCESS).
** Trained on GCP.
** Summary of clinical safety/Narrative Writing.
** Data management (Safety database)Medical stats & Meta analysis
** Source doc.verfication and crf review, Scientific reviewing
** Regulatory review (MEDRA)/regulatory documentation
** Adverse event& (SAE) reporting and follow up/evaluating safety reports
** CRF tracking
** Cinical database activities and updation.
** Domain presentation/seminar/During meetings.
** Regulatory aspect of medical writing / study audits
** Clinical safety ( product )/Devices
** Evaluation of clinical adverse events as per prescribing information, package insert etc.
** Research and review on medical queries and information
** Safety surveillance
** Answering medical queries /Information.
** Analysis and reporting clinical data and information(Clinical- Documentation, Presentation
** Clinical operation ‘s statistic data management and crf to resolve data queries(reporting)
** crf’s and crf completion guidelines.
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Worked with pfizer india (post M. pharm-Product management includes clinical research and application) [April-2002 to Dec 2005 Includes Project work during M.pharm ] and worked with kare pharmaceuticals (post Diploma)[may-96 to may 97 (Apprenticeship-Mandatory)

Job profile :
** Basics of clinical trials and clinical research
** Features of clinical trials,clinical pharmacology,non clinical pharmacology and toxicology.
** Good clinical trial practice .
** Safety surveillance/pharmacovigilance
** Source document verification
** Data management and study documentation.
** Clinical operations,statistics’data management and crf design for data queries and reporting.( 21 cfr part ii )
** Safety reporting, tracking and review
** Summary of clinical safety
** Promoting Pfizer drugs and answering Queries related to product.

ACHIEVEMENTS :
** Participated in mathematics olympiad merit certificate winner
** Participated in debate and declamation (inter college)participated in debate and quiz during ipa functions.
** Won grand slam trophy during pfizer`s daxid (ssri) launch for best detailing (west zone); displayed live on cnn.
** To conduct (CME) continuous medical education for doctors and other medical fraternity; and have also given several power point presentation .
** Was live on CNN to launch daxid (SSRI)and was given apprecition letter and trophy by the foreign delegates .

Personal Details :
NAME : Mr. Varinder singh
FATHER`S NAME : Late. Mr. Raghubir singh
DATE OF BIRTH : 17 JUN. 1977.
MARITAL STATUS : Married.
TELEPHONE : cell no:9930125448.
E-MAIL ID : varinder22 AT rediffmail.com. Varinder22 AT gmail.com
NATIONALITY : INDIAN.
LANGUAGES KNOWN : English, Hindi, Marathi & Punjabi.
HOBBIES : Reading books, traveling,listening music etc.
EXTRA CURRICULAR ACTIVITIES : Won prizes & certificates in sports & games.
ASSETS : Willing to learn,hard working, extrovert in nature, a burning desire to excel.
ADDITIONAL QUALIFICATION : DONE BASIC COURSE IN COMPUTER.

Expecting an oppurtunity to serve your esteemed organization

Varinder singh


 

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