CV, India Based Graduate With 3 years' Experience In Pharmacovigilance

Available
Serial No: 19197
Skills keywords: meddra, pharmaceutical science, who-dd

Short Bio:

I am Pharma graduate with 3 years of expereience in Pharmacovigilance. Knowledge of MedDRA, WHO-DD, Currectly i am working as Quality reviewer for serious and Non Serious spontaneous cases. I have an experience in ARGUS and ARIS-g database. Knowledge of different types of cases such as pregnancy cases, device related cases and spotaneous cases. Worked in diferent therapeutics area such as OTC, Contraceptives, Antihypertensives and Renal. I am a quality reviewer and case finalizer working on Aris

Current location:  Karnataka, India - View on map
Nationality: Indian
Preferred Sector of Employment:  Pharmaceutical and Science
Spoken languages: english, Hindi, KANNADA, marathi, Telugu
Location I am interested in working: Anywhere

Qualifications

Education – Year of Passing – Institution –  Percentage

M. Pharm (Pharmaceutics) 2011 Bharati Vidyapeeth college of Pharmacy, Kolhapur(M.S) 68%

B. Pharm 2009 Sudhakarraonaik Institute of Pharmacy, Pusad(M.S) 66.70%

H.S.C. 2004 Anandniketan college,Warora(M.S) 67%

S.S.C. 2002 Manikgarh cement school, Gadchandur (M.S) 71.86%

Career Summary

1) Worked in TATA CONSULTANCY SERVICES LIMITED from 12-Feb-2012 to 03-Sep-2013 as a senior process associate.

2) Working in SYNOWLEDGE INDIA PVT LTD as senior drug safety associate as quality reviewer from 10-Sep-2013 till date.

ORGANISATION: TATA CONSULTANCY SERVICES LIMITED:

ROLE: Senior process associate

• Worked on ARGUS Database.

• Handled litigation, spontaneous and pregnancy cases.

• Responsible for case intake and triaging the cases as per seriousness into their workflow

• Worked on different therapeutic class ex) contraceptives and OTC.

• Handle responsibilities of developing concise, accurate and well-written case narratives

• Knowledge of MedDRA and WHODD with coding of medical history and events.

ORGANISATION: SYNOWLEDGE INDIA PVT LIMITED:

ROLE: Senior drug safety associate

• Worked on Aris-g database.

• Quality review of case pushed into QC workflow.

• Take quality improvement session to increase the quality of DE associates.

• Mentor new associates

• Create new follow up of a case based on the new information received.

• Send clarification mail for information provided in the case.

 

AREA OF INTEREST:

Pharmacovigilance and regulatory affairs

 

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