my_resume -peeyush kumar shrivastava- updated

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CURRICULUM VITAE Page 1 of 4 - 1 - Curriculum Vitae Name: PEEYUSH KUMAR SHRIVASTAVA Academic Qualification(s) MSc. BPT Address (Name of Institution, Street, City, Postal Code, State or Province (if applicable), Country): Department of Surgical Gastroenterology & Human Organ Transplant King George Medical University, Lucknow Chowk, Lucknow-226003, UP, (India) Contact number/ Email ID: Mo No. 09335156066, 9451445749 [email protected] Education and Training (List all Colleges, Universities and Medical Schools attended incl. postdoctoral/fellowship training, including board certification/medical license): Name and Location of Institution (City, State or Province and Country) Degree and Year Awarded Area of Study UP Rajarshi Tandon Open University MSc,2013 Biochemistry Allahabad Agricultural University, Allahabad, UP, India BPT, 2007 Physiotherapy Lucknow Christian Degree College, Lucknow BSc., 2002 Zoology, Botany, Chemistry Professional Experience :

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Page 1: MY_RESUME -Peeyush Kumar Shrivastava- updated

CURRICULUM VITAE Page 1 of 4

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Curriculum Vitae

Name: PEEYUSH KUMAR SHRIVASTAVA

Academic Qualification(s) MSc. BPT

Address (Name of Institution, Street, City, Postal Code, State or Province (if applicable),

Country):

Department of Surgical Gastroenterology & Human Organ Transplant

King George Medical University, Lucknow

Chowk, Lucknow-226003, UP, (India)

Contact number/ Email ID:

Mo No. 09335156066, 9451445749

[email protected]

Education and Training (List all Colleges, Universities and Medical Schools attended incl.

postdoctoral/fellowship training, including board certification/medical license):

Name and Location of Institution

(City, State or Province and

Country)

Degree and Year

Awarded Area of Study

UP Rajarshi Tandon Open University

MSc,2013

Biochemistry

Allahabad Agricultural University,

Allahabad, UP, India

BPT, 2007

Physiotherapy

Lucknow Christian Degree College,

Lucknow

BSc., 2002

Zoology, Botany,

Chemistry

Professional Experience :

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CURRICULUM VITAE Page 2 of 4

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Position/Title

Name and Location of

Institution

(City, State or Province

and Country)

Dates

(Start/Stop Dates as

applicable)

Human Organ Transplant

Coordinator

KGMU, Lucknow, UP

(India)

2013-Continued

Clinical Research Coordinator KGMU, Lucknow., UP

(India)

2007-Continued

Physiotherapist Surgical Nursing Home

Sec. G -LDA colony

Kanpur road Lucknow

2008-Continued

Observer Physiotherapist Vivekananda Polyclinic,

Ramakrishna Mission

Sevashram Lucknow

2006-2007

Internship Lal Hospital and Research

Center Kanpur Road

Lucknow

2007-2008

Previous participation in clinical trials:

Indication of Trial Clinical

Phase of

Trial (I-IV)

Role in Trial (e.g.

Investigator, Sub-

Investigator)

Year in which trial was

conducted (Start/Stop

Dates)

IBS with Constipation

Phase III Study Coordinator 2015-2016

COPD

Phase III Study Coordinator 2012-2015

Community Acquired

Pneumonia

Phase III Study Coordinator 2011-2012

Active Moderate

Ulcerative Colitis

Phase III Study Coordinator 2010-2011

Chron’s Disease Phase III Study Coordinator 2009-2010

VTE prophylaxis in

major abdominal

surgery

Phase III Study Coordinator 2009-2010

Active Moderate Phase III Study Coordinator 2009-2011

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Ulcerative Colitis

Inoperable Gastric and

Gastro Oesophageal

Cancer

Phase III-b Study Coordinator 2008-2012

Gastro Oesophageal

Reflux Disease

Phase III Study Coordinator 2008-2009

Post Operative Ileus

Phase III Study Coordinator 2007-2008

Reflux Oesophagitis Phase IV Study Coordinator 2007-2008

Specific responsibilities include:

Creation of Standard Operating Procedures for each study or clinical trial.

Responsible for communication with central and local IRBs and maintaining ethical

approval for studies, from initial study approval through study amendments, annual

continuations, and finally termination.

Maintenance of source documents and regulatory documentation of clinical trial. Ensure

quality of data on CRFs.

Preparation of documents for review by sponsors, monitors and regulatory authorities, as

necessary.

Recruitment of subjects

Screening and scheduling subjects visits

Processing and shipping lab work

Ensure subject safety and adverse event reporting to sponsor and IRB/IEC.

Maintaining study-specific supplies

Maintaining drug accountability logs and storage requirements.

Experience of working with various eCRF formats like – DATA LABS, RAVE,

iMEDIDATA, RDC, ACEELIANT

Experienced in using computerized information systems, Word, Excel, PowerPoint, and

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CTMS required.

Monitoring of health and safety of subjects with frequent contact and ensure subject

compliance with the study protocol.

Adverse event documentation to Principal Investigator and sponsor where appropriate.

Participation in meetings with sponsors, monitors and regulatory authorities, as necessary

Training and Workshops:

IM attends:

End of Study Meeting in organized in HONGKONG in 2016 organised by Glaxo Smith

Cline in COPD study

Study Coordinator meeting Organized in Taiwan in 2014 Organised by Glaxo Smith

Kline in COPD Study

Investigator meeting held in Bangalore Organized by Astrazeneca in 2012 India Pvt.

Ltd. in Pneumonia study

Investigator meeting held in Chennai in 2009 Organized by ICON Clinical Research

Organisation in Venous Thrombo Embolism study.

Workshops attend:

Transplant Coordinator Training workshop at Fortis Hospital Gurgaon in Association

with “Mohan Foundation’ New Delhi.

ICH GCP workshop in 2011organized by King George’s Medical University Lucknow.

ICH GCP workshop in 2010 organized jointly by Pfizer and King George’s Medical

University Lucknow.

Achievement:

Awarded as “Star Study Coordinator” of the month in March 2009 in the Oncology study

(Inoperable Gastric and Gastro oesophageal Carcinoma) by, “Thrombosis Research

Institute” (TRI) on recruitment of 52 patients of Upper Gastro Intestinal Cancer in one

year..

Signature: Date 06/04/2016