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SACHIN KUMAR C/O-Sh.

Tara Chand
1449/22A Gali no-10 Gandhi Marg,
Durga Puri Shahdara,PIN:- 110093
Email: sonuniper@gmail.com

PROFESSIONAL SUMMARY:
Total 4 years 8 months of professional experience of which 1year as a Lecturer in pharmacology & 3 years 8
months in pharmacovigilance. Knowledge of saf et y study requirement for clinical development process.
Managing trainees in adverse event collection, p r o c e s s i n g & e n t r y o f ICSRs. Well v er s e d i n
ADR processing, writing case narratives and case follow-up. Coordinating Vigiflow training and liaise with
pharmacovigilance centres and CDSCO. Familiar with applicable guidelines to clinical research,
pharmacovigilance. An effective communicator with analytical, problem solving and organisational skills. Possess
a self motivated, flexible and detail oriented attitude.

CORE COMPITENCIES:

Team management in adverse event collection, processing and entry

Spontaneous adverse event case processing and reporting.

Coding/recoding of terms using WHO-DD and WHO-ART.

Aggregate reporting and quality check of ICSR.

Vigiflow implementation, training and technical support.

Interfaces with physician in case follow-up.

Medical literature search and writing case narratives.

Proficient in MS office word, excel, power point, access and project.

EDUCATION

2007 2009 M.S (Pharm.) PharmacoinformaticsNational Institute of Pharmaceutical Education
& Research (NIPER)

2004 - 2007 B. Pharma
Kedar Nath Modi Institute of Pharmaceutical Education & Research, (KNMIPER),
Modinagar, U.P

2002-2004 D. Pharm
Chotu Ram Rural Institute of Technology (CRRIT), Delhi

OTHER QUALIFICATION
Post Graduate Diploma in Clinical Research from Catalyst clinical services
Proficiency programme in Pharmacovigilance from Bioinformatics Institute of India
Post graduate Diploma in Pharma regulatory affairs from Bioinformatics Institute of India

PROFESSIONAL EXPERIENCE
Technical Associate: September 2012 to till date (AI I MS, New Delhi)
ADR Monitoring Centre (AMC), Pharmacovigilance Programme of India (PvPI), All India Institute of
Medical Sciences (AIIMS), New Delhi
Funded by Ministry of Health and Family Welfare, Govt. of India.
TASKS & RESPONSIBILITIES SHARED AT AIIMS

Collection of adverse events from hospital wards and perform causality assessment as per
WHO-UMC and Naranjos scale
Coding of drugs and events as per WHO-DD, WHO-ART and data entry in excel format for
analysis, information retrieval and duplicate report removal.
Preparing aggregate reports of data received from peripheral centre and submitting to
CDSCO
Evaluation of PSUR/PMS reports and providing support to CDSCO

Technical Associate: September 2010 to August 2012(GMC, J ammu)
ADR Monitoring Centre (AMC), Pharmacovigilance Programme of India (PvPI), Government Medical
College (GMC), Jammu
Funded by Ministry of Health and Family Welfare, Govt. of India.

TASKS & RESPONSIBILITIES SHARED AT GMC,JAMMU

Managing trainees in data collection and entry of ICSR in Vigiflow as per SOPs.

Providing training in case processing of all reported events and SAEs.

Reviewing, classification of events and ensuring completeness and quality.

Performing case follow-up and writing case narratives.

Periodic aggregate data reports of drugs under focused monitoring system.

Assisted in preparation of SOPs for the Pharmacovigilance Programme of India.

Vigiflow training of postgraduate students

Pharmacology Lecturer: September 2009 - September 2010

Kedar Nath Ginni Devi Modi Institute of Pharmaceutical Education & Research, Modinagar, U.P

Visiting faculty of Clinical Research & Pharmacovigilance: J uly 2009 to J uly 2010

Bioinformatics Institute of India , Noida

Visiting faculty of Pharmacovigilance: September 2012 to till date

Indian biosciences & Research Institute, Noida


EXPERIENCE AND TRAINING
1. Industrial Tour
Name of Organization : TC Health Care, Ghaziabad, UP.
Project Undertaken : Manufacturing of Tablets, Capsules and Syrups.

2. Industrial Training
Name of Organization : DABUR, Ghaziabad, U.P.
Duration : 1 month

3. Hospital Training
Name of hospital : SDNH Shahdara.
Duration : 3 months
DISSERTATION/ THESIS
Research Project entitle: Modeling of Multi Drug resistance protein of leishmania donovani and Insilco
prediction of active drugs.

Organization: Rajendra Memorial Research Institute of Medical Sciences (RMRIMS), Patna.
Duration: January 2009 to June 2009 (6 months).



REVIEW ARTICLE
Ekta Arora, Vijay Khajuria, Sachin Kumar*, Z.Gillani, Shamiya Sadiq, V R Tandon., Stevia: A

Promising Herbal Sweetener.J K Science Vol. 12 No. 4, Oct-December 2010.


EDITORIAL `
Vishal R. Tandon, Sudhaa Mahajan*, Annil Mahajan**, Sachin Kumar.,Pharmacovigilance Centres in

Detection of Medication Errors and Ensuring Patient Safety. Vol. 13 No. 4, Oct-December 2011.

Sudhaa Mahajan*, Vishal R. Tandon, Sachin Kumar., Women & Risk For Developing ADRs. Vol. 14
No. 1, J anuary-March 2012.

ABSTRACTS


Vishal R Tandon , Ekta Arora, Z. Gillani, V.Khajuria, Brij Mohan Gupta, Shamia Sadiq, Ajay Dogra,
Sachin Kumar, Vivek Mahajan, Rajesh Koul, Bharat Bhushan, Samir Hamid Zargar, Aman Sharma, Sapna
Arora, Kiran Kapoor, Prem Lata., One year experience of Drug Information Centre and OPD of a
Tertiary Care College from Northern India.3
RD
National Conference ISRPTCON 2011 Jammu
(Abstract no. PP-51, pp-71) at Department of Pharmacology and Therapeutics, Govt. Medical College,
Jammu, 25
th
-27
th
November 2011.
Vishal R Tandon, Shamia Sadiq, Sachin Kumar, Z. Gillani, V.Khajuria, Brij Mohan Gupta, Ekta Arora,
Ajay Dogra, Vivek Mahajan, Rajesh Koul, Samir Hamid Zargar, Bharat Bhushan, Aman Sharma, Sapna
Arora, Kiran Kapoor, Prem Lata., Evaluation of the Knowledge ,Attitude and Practices on Adverse
Drug Reactions and Pharmacovigilance Among Healthcare Professionals from Tertiary Care College
from Northern India.3
RD
National Conference ISRPTCON 2011 Jammu (Abstract no. PP-51, pp-94) at
Department of Pharmacology and Therapeutics, Govt. Medical College, Jammu, 25
th
-27
th
November 2011.


STUDIES SUPERVISED


Prescriptions trend analysis of various prescriptions originating in Out Patients department of AIIMS: A

cross-sectional observational study.

Causality Assessment of ADR reports of Anti Epileptic Drugs received at ADR Monitoring Centre, Dept.

of Pharmacology, AIIMS, New Delhi: and Pilot Study of Prescription hand writing analysis

To evaluate the adverse drug reaction due to levetiracetam in Indian patients with epilepsy: An observational
and cross sectional study.
An observational and cross sectional study to evaluate the effects of levetiracetam on mood, behavior and
sleep in patients with epilepsy
Quality Assessment of ADR reports of Rituximab received at ADR Monitoring Centre, Dept. of

Pharmacology, AIIMS, New Delhi & Focused Pharmacovigilance of Rituximab in AIIMS


ACADEMIC ACHIEVEMENTS

Selected for All India Niper Entrance Exam-2007, conducted by Niper Mohali.

Qualified GATE-2006 in the discipline of Pharmaceutical Sciences.

Honors in pharmacy by U.P Technical University.

DPC Awarded (DELHI PHARMACY COUNCIL).

Awarded Monthly Scholarship From Ministry of Chemical and Fertilizers (Government of India), New

Delhi, India, during M.S Pharm. (Pharmacoinformatics) Session (2007-09).

Previously working In Govt. Medical College Jammu as a Technical Associate UNDER CDSCO (Central

Drug Standard Control Organization).

Presently working in AIIMS as a Technical Associate UNDER IPC (Indian Pharmacopoeia Commission)
From Dated: - 01-Sep-2012 to till date .

2 years of Experience in Collecting, Accessing and Monitoring of ADR Data in GMC, Jammu.

Total experience of 3 years 8 month in Pharmacovigilance.

Conduct Training session of Vigiflow software for MD students of Govt. medical college, GMC, Jammu.


INVITING LECTURE

Invited as a Guest Lecturer for Pharmacovigilance in Pharmacy College K.N.M.I.P.E.R (Modi

Foundation), Modinagar, U.P

Invited as a Guest Lecturer for Pharmacovigilance Bioinformatics Institute of India (Institute of Clinical

Research), Noida.


CONFERENCES/ WORKSHOPS / TRAINING SESSIONS ATTENDED:

Attended Mini Symposium on Current Regulatory Frame Work In Clinical Trials organized by Clinical
Research Advancement Towards Excellence (CREATE) Center, Department Of Pharmacology AIIMS, New
Delhi, 25- April- 2014.

Attended 1 day Symposium on Patient Safety and Clinical research organized by Clinical Research
Advancement towards Excellence (CREATE) Center, Department Of Pharmacology AIIMS, 18-March -2014.

Attended 1 day Mini Symposium On PHARMACOVIGILANCE AND MEDICINE SAFETY, organized by Clinical
Research Advancement Towards Excellence (CREATE) Center, Department Of Pharmacology AIIMS,Date: 19
th
March
2014.

Attended 1 day workshop on AIIMS Capacity Building Workshop on Pharmacovigilance in Clinical Trials
organized by Clinical Research Advancement Towards Excellence (CREATE)Center, Department of
Pharmacology AIIMS, New Delhi, 16
th
July 2013

WHO-UMC - AIIMS Vigiflow advanced training course on reporting and management, 23 February 2011,
New Delhi.

WHO-UMC - AIIMS Vigiflow training course on report entry and management, 24-25 November 2010, New
Delhi.

Attended 3 Days 3
rd
National Conference ISRPTCON 2011 Jammu at Govt. Medical College, Jammu.

Attended Conference on Pharmacovigicon-2010 under ISRPT.

WHO-UMC - PGI one day Training Programme for Technical Associates (TAs) of Northern Zone of India on
Causality Assessment and Vigiflow on 21-01-2012.

PERSONAL

Date of Birth : 18-AUG-1984
Fathers Name : Mr. Tara Chand
Gender : Male
Marital Status : Single
Languages Known : English, Hindi
Nationality : Indian

REFRENCES

Prof YK Gupta, Head, Department of Pharmacology, All India Institute of Medical
Sciences (AIIMS), Ansari Nagar, New Delhi. Email: yk.ykgupta@gmail.com

Prof Zahid Gillani, Head, Department of Pharmacology, Government Medical College,
Jammu. Email: drzgillani@rediffmail.com


DECLARATION



I, hereby declare that all the information given above is correct to the best of my knowledge.


Place :

Dated :

(SACHIN KUMAR)

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