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PIYUSH KUMAR
1348/19C/1, St. N. 8
Rishi Nagar Extention,
Haibowal Khurd
Ludhiana, Punjab, 141001
E-mail: piyushdav@yahoo.co.in
Phone: +91-9915696362, +919425390512
Career Objective
 Establish a career in the Clinical Research industry as a Clinical Research Professional by implementing
my technical knowledge and experience of Clinical Research Coordinator
Work Experience
o Working as a Clinical Research Coordinator at, Dayanand Medical College and Hospital,
Ludhiana, Punjab since 1st Dec 2009 to present
o Job Responsibilities
 To help investigator in screening of subjects
 To assist in informed consent process
 To keep IP accountability
 To complete the CRF
 To dispense drug to the subjects
 To document the source note and source data
 To complete the eCRF
 To do IVRS for subject’s randomization in randomization studies
 To ensure compliance of project specific schedule of activities
 Preparation, attendance and follow-up of monitoring
 Completing CRF entry with minimal error.
 Preparation, attendance and follow-up of Audit
 Trial closeout: preparation, attendance and follow-up; forwarding the necessary information of
site closeout to all concerns
 To complete and update various logs used in study
 To make coordination with PI, Monitor, Subjects, lab personnel and vendors
 To maintain the documents in Investigator Site File
 To submit SUSARs and SAEs to Ethics Committee
 To attend the Institutional Ethics Committee Meeting
Clinical Phase
of the trial (I –
IV)
Indication of the trial Role in trial
(e.g. Principal
Investigator,
Co – Investigator etc)
Year in which trial was conducted
III HEPATITS C Clinical Research
Coordinator
2012 – Ongoing
III HEPTITIS C Clinical Research
Coordinator
2012
Observational HEPATITIS C and B Clinical Research
Coordinator
2012
II B HEPATITIS C Clinical Research
Coordinator
2011-2012
IV ULCERATIVE COLITIS Clinical Research
Coordinator
2011 -2012
III ULERATIVE COLITIS Clinical Research
Coordinator
2010-2011
III ULCERATIVE COLITIS Clinical Research
Coordinator
2009-2010
 Neurology of Celiac Disease : A hospital Based Study of the Celiac Disease and Prevalence of Celiac Disease in
Epilepsy – Junior Research Fellow
Certification
 Online base SAS from Grassroots Consulting Pvt. Ltd. (June 2016)
 ICH GCP training organized by Research and Development Centre, Dayanand Medical College and Hospital,
Ludhiana, 24 Feb 2015
 Online training for reporting SAE’s using Inform Rev 1.00 from Merck & Co. (09 Aug 2012)
 Informed Consent Process eLearning Course From Merck & Co. (08 Aug 2012)
 Online ICH GCP training from Merck & Co. (03 Aug 2012)
 Online training on Inform v 4.6 for CRC and for PIs performing data entry and eSignature from Merck and Co. (
08 Jul 2012)
 Online Medidata Rave EDC Research Coordinator Training (15 May 2012)
 Online High quality IATA Training for Shipping Biological Substances, Infectious Substances and Related
Hazards(30 Apr 2012)
 Online ICH GCP Guidelines from SPD476-409 (15 Feb 2012)
 Online EXT120 DataLabs® v 4.6 Investigator Training (10 Jan 2012)
 Certificate course in Clinical Nutrition ( March 2011)
 Online PDS Express Electronic Data Capture System training from Phoenix Data System( Feb
2010)
 One year full time Advance Post Graduate Diploma in Clinical Research (APGDCR) from Clinical
Research Education and Management Academy (CREMA) New Delhi (2008-2009)
 One year online diploma in Clinical Research Associate from Clinical Research International,
Canada (2008-2009)
 Open Access GCP test on Pharmaxm.com (August, 2009)
Workshops and Conferences
 Attended 5th National IBD MEET September 12th - 13th, 2015 at Chandigarh
 Workshop on Scientific Paper Writing in 69th Annual conference of association of Physicians of India
19th Feb 2014, at DMC&H, Ludhiana
 Attended 3nd National IBD Meet, 29th and 30th Sep 2012, Gurgaon
 Attended 2nd National IBD Meet, 23rd May2010, The Oberoi, New Delhi
 Attended Asian Summit on clinical trials, 19th – 20th may 2009, New Delhi
 Participated in workshop on subject enrollment and retention in clinical trials by Diana Anderson and
Company, 2008
Achievements
 Successfully screened and randomized 11 subjects within very short period of time
 Successfully counseled the patients and prevented screen failure and dropouts
 Developed skills to manage all the documents related to trial to get approval from ethics committee
Project
 Effect of Parthenin (Parthenium spp.) on germination and growth of seeds of pulses and cereals
Educational Qualification
 B.Ed. : DDU Gorakhpur University, Gorakhpur U.P.(2005)
 M.Sc. : Botany, Allahabad University, Allahabad, U.P.(2002)
 B.Sc. : Botany, Zoology, Chemistry, Allahabad University, Allahabad, U.P (2000)
Computer Skills
 O/S WIN 98/XP, MS Office 2000/2007
Hobbies and Interests
 Travelling, Net Browsing, Painting and Cooking
Declaration
I hereby declare that the information furnished above is true to the best of my knowledge.
Date:
Place: Ludhiana ____________________
Piyush Kumar

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Piyush Kumar 26_02_2016

  • 1. PIYUSH KUMAR 1348/19C/1, St. N. 8 Rishi Nagar Extention, Haibowal Khurd Ludhiana, Punjab, 141001 E-mail: piyushdav@yahoo.co.in Phone: +91-9915696362, +919425390512 Career Objective  Establish a career in the Clinical Research industry as a Clinical Research Professional by implementing my technical knowledge and experience of Clinical Research Coordinator Work Experience o Working as a Clinical Research Coordinator at, Dayanand Medical College and Hospital, Ludhiana, Punjab since 1st Dec 2009 to present o Job Responsibilities  To help investigator in screening of subjects  To assist in informed consent process  To keep IP accountability  To complete the CRF  To dispense drug to the subjects  To document the source note and source data  To complete the eCRF  To do IVRS for subject’s randomization in randomization studies  To ensure compliance of project specific schedule of activities  Preparation, attendance and follow-up of monitoring  Completing CRF entry with minimal error.  Preparation, attendance and follow-up of Audit  Trial closeout: preparation, attendance and follow-up; forwarding the necessary information of site closeout to all concerns  To complete and update various logs used in study  To make coordination with PI, Monitor, Subjects, lab personnel and vendors  To maintain the documents in Investigator Site File  To submit SUSARs and SAEs to Ethics Committee  To attend the Institutional Ethics Committee Meeting Clinical Phase of the trial (I – IV) Indication of the trial Role in trial (e.g. Principal Investigator, Co – Investigator etc) Year in which trial was conducted III HEPATITS C Clinical Research Coordinator 2012 – Ongoing III HEPTITIS C Clinical Research Coordinator 2012 Observational HEPATITIS C and B Clinical Research Coordinator 2012 II B HEPATITIS C Clinical Research Coordinator 2011-2012 IV ULCERATIVE COLITIS Clinical Research Coordinator 2011 -2012 III ULERATIVE COLITIS Clinical Research Coordinator 2010-2011 III ULCERATIVE COLITIS Clinical Research Coordinator 2009-2010
  • 2.  Neurology of Celiac Disease : A hospital Based Study of the Celiac Disease and Prevalence of Celiac Disease in Epilepsy – Junior Research Fellow Certification  Online base SAS from Grassroots Consulting Pvt. Ltd. (June 2016)  ICH GCP training organized by Research and Development Centre, Dayanand Medical College and Hospital, Ludhiana, 24 Feb 2015  Online training for reporting SAE’s using Inform Rev 1.00 from Merck & Co. (09 Aug 2012)  Informed Consent Process eLearning Course From Merck & Co. (08 Aug 2012)  Online ICH GCP training from Merck & Co. (03 Aug 2012)  Online training on Inform v 4.6 for CRC and for PIs performing data entry and eSignature from Merck and Co. ( 08 Jul 2012)  Online Medidata Rave EDC Research Coordinator Training (15 May 2012)  Online High quality IATA Training for Shipping Biological Substances, Infectious Substances and Related Hazards(30 Apr 2012)  Online ICH GCP Guidelines from SPD476-409 (15 Feb 2012)  Online EXT120 DataLabs® v 4.6 Investigator Training (10 Jan 2012)  Certificate course in Clinical Nutrition ( March 2011)  Online PDS Express Electronic Data Capture System training from Phoenix Data System( Feb 2010)  One year full time Advance Post Graduate Diploma in Clinical Research (APGDCR) from Clinical Research Education and Management Academy (CREMA) New Delhi (2008-2009)  One year online diploma in Clinical Research Associate from Clinical Research International, Canada (2008-2009)  Open Access GCP test on Pharmaxm.com (August, 2009) Workshops and Conferences  Attended 5th National IBD MEET September 12th - 13th, 2015 at Chandigarh  Workshop on Scientific Paper Writing in 69th Annual conference of association of Physicians of India 19th Feb 2014, at DMC&H, Ludhiana  Attended 3nd National IBD Meet, 29th and 30th Sep 2012, Gurgaon  Attended 2nd National IBD Meet, 23rd May2010, The Oberoi, New Delhi  Attended Asian Summit on clinical trials, 19th – 20th may 2009, New Delhi  Participated in workshop on subject enrollment and retention in clinical trials by Diana Anderson and Company, 2008 Achievements  Successfully screened and randomized 11 subjects within very short period of time  Successfully counseled the patients and prevented screen failure and dropouts  Developed skills to manage all the documents related to trial to get approval from ethics committee Project  Effect of Parthenin (Parthenium spp.) on germination and growth of seeds of pulses and cereals Educational Qualification  B.Ed. : DDU Gorakhpur University, Gorakhpur U.P.(2005)  M.Sc. : Botany, Allahabad University, Allahabad, U.P.(2002)
  • 3.  B.Sc. : Botany, Zoology, Chemistry, Allahabad University, Allahabad, U.P (2000) Computer Skills  O/S WIN 98/XP, MS Office 2000/2007 Hobbies and Interests  Travelling, Net Browsing, Painting and Cooking Declaration I hereby declare that the information furnished above is true to the best of my knowledge. Date: Place: Ludhiana ____________________ Piyush Kumar