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CURRICULUM VITAE
VINOTH KAMBLI.K Contact Details
Clinical Research Associate (2 years’ Experience) Email : kambli.k89@gmail.com
Mobile : +919677340846.
OBJECTIVE:
 To pursue a career in a progressive, dynamic and challenging environment with opportunities for
growth and obtain a position that will enable me to use my strong organizational skills, work
experience, educational background, and ability to work well with people.
STRENGTHS:
 Good Communication and Writing Skills.
 Self-motivated, Hardworking and Adaptable.
 Patience and Confidence.
EDUCATIONAL QUALIFICATIONS:
Name of Courses College/University Year
B.TECH
(BIOTECHNOLOGY)
Sri Venkateswara college of Engineering, Chennai. 2010 – 2013
Diploma (D.CH.E)
Chemical Engineering
Sembodai R.V.Polytechnic College, Sembodai. 2008 – 2010
WORK EXPERIENCE:
Name of Organization Designation Year
Quest Life Sciences Pvt,Ltd. Clinical Research Associate Dec-2013 to Dec-2015
Role: Clinical Research Associate
 Ensuring that allBio-Study Related Activities are Recorded,Conducted and Reported in Accordance
with Standard Operating procedures(SOPs), Protocol,Good ClinicalPractice (GCP),and the Relevant
Regulatory Requirements.
 Prepare and Review Regulatory Documents such as Investigator’s Brochure, Clinical Trial
Protocol, Informed Consent Document and Case Report Form & Clinical Study Report.
 Conduct and Monitoring of clinical study in compliance to Protocol, SOP,ICH-GCP and other
applicable Regulatory requirement.
 To ensure allthe activities are carried out in accordance with study Protocol. Preparing,modifying and
review of Standard Operating procedures(SOPs.
 Perform Monitoring and auditing visits at Clinical Sites and Preparation of Clinical SOPs and
maintain QA documentation.
 Ensuring the preparation of Case Report Forms (CRFs)in accordance with Protocol.
 Compilation of Case Report Form and Trial Master File.
 Maintains subject screening logs and protocol deviation logs.
 Recording the data generated during study in Case Report Forms.
 Involved in activities such asDrug administration,Sample processing,MealDistribution,Check-in and
Check-out of subjects,ensuring subject well-being.
 Contribute to the preparation of the clinical study report.
 Review and finalization of documents such as site feasibility report, site qualification report, site
monitoring report, and site closeout report.
 Provide updates and status reports on ongoing clinical trials.
 Coordinates and facilitates monitoring and auditing visits.
 Notifies appropriate institutional officials of external audits by CROs and sponsors.
 Assists the Principal Investigator in submission of accurate and timely closeout documents.
ACHEIVEMENTS:
 Actively Participated in the Seminar NATIONAL LEVEL SEMINAR ONTRENDS AND
PERSPECTIVES IN BIOTECHNOLOGY Organized by Sri Venkateswara college of
Engineering.
TRAINING:
 Actively Participated in the Training on GOOD CLINICAL PRACTICES at Quest Life
Sciences PVT LTD, Chennai.
 Actively Participated in the Training on BASIC LIFE SUPPORT TRAINING PROGRAM at
Quest Life SciencesPVT LTD, Chennai.
 Actively Participated in the Training on BASIC LIFE SUPPORT TRAINING PROGRAM
at MEHTA HOSPITALS PVT LTD, Chennai.
AREA OF INTEREST:
 Clinical Research Associate
 Clinical Trials
 Clinical Data Coordinator
 Clinical Data Management
 Quality Control & Quality Assurance.
KEYSKILLS:
 Effective oral and written communication skills
 Excellent interpersonal skills
 Strong attention to detail
 Basic computer skills and the ability to learn appropriate software
 Good English language and Communication skills
 Ability to work in a team or independently as required
 Ability to travel and spend 60 to 80%ofworking week at site
 Basic software and computer skills,including MS Office applications
PERSONAL DETAILS:
Fathers Name : Kirubakaran.R
Date of birth : 15th
December 1989
Nationality : Indian
Gender : Male
Marital status : Unmarried
Languages known : English, Tamil & Hindi.
Present Address : 2070/1, Subham Apartments, 5th Street, Nehru Nagar, 13th Main Road,
Anna Nagar, Chennai-600040.
Permanent Address : 2/154, Mangudi, South Street, Thirumangalam (PO),
Mayiladuthurai (TK), Nagapattinam (DT)-609811.
Mobile : +919677340846 & 8452866323.
Email ID : kambli.k89@gmail.com
DECLARATION:
 I hereby declare that the above-mentioned information is correct up to my knowledge and I bear
the responsibility for the correctness of the above-mentioned particulars.
Date: Signature

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vinoth new (1)

  • 1. CURRICULUM VITAE VINOTH KAMBLI.K Contact Details Clinical Research Associate (2 years’ Experience) Email : kambli.k89@gmail.com Mobile : +919677340846. OBJECTIVE:  To pursue a career in a progressive, dynamic and challenging environment with opportunities for growth and obtain a position that will enable me to use my strong organizational skills, work experience, educational background, and ability to work well with people. STRENGTHS:  Good Communication and Writing Skills.  Self-motivated, Hardworking and Adaptable.  Patience and Confidence. EDUCATIONAL QUALIFICATIONS: Name of Courses College/University Year B.TECH (BIOTECHNOLOGY) Sri Venkateswara college of Engineering, Chennai. 2010 – 2013 Diploma (D.CH.E) Chemical Engineering Sembodai R.V.Polytechnic College, Sembodai. 2008 – 2010 WORK EXPERIENCE: Name of Organization Designation Year Quest Life Sciences Pvt,Ltd. Clinical Research Associate Dec-2013 to Dec-2015
  • 2. Role: Clinical Research Associate  Ensuring that allBio-Study Related Activities are Recorded,Conducted and Reported in Accordance with Standard Operating procedures(SOPs), Protocol,Good ClinicalPractice (GCP),and the Relevant Regulatory Requirements.  Prepare and Review Regulatory Documents such as Investigator’s Brochure, Clinical Trial Protocol, Informed Consent Document and Case Report Form & Clinical Study Report.  Conduct and Monitoring of clinical study in compliance to Protocol, SOP,ICH-GCP and other applicable Regulatory requirement.  To ensure allthe activities are carried out in accordance with study Protocol. Preparing,modifying and review of Standard Operating procedures(SOPs.  Perform Monitoring and auditing visits at Clinical Sites and Preparation of Clinical SOPs and maintain QA documentation.  Ensuring the preparation of Case Report Forms (CRFs)in accordance with Protocol.  Compilation of Case Report Form and Trial Master File.  Maintains subject screening logs and protocol deviation logs.  Recording the data generated during study in Case Report Forms.  Involved in activities such asDrug administration,Sample processing,MealDistribution,Check-in and Check-out of subjects,ensuring subject well-being.  Contribute to the preparation of the clinical study report.  Review and finalization of documents such as site feasibility report, site qualification report, site monitoring report, and site closeout report.  Provide updates and status reports on ongoing clinical trials.  Coordinates and facilitates monitoring and auditing visits.  Notifies appropriate institutional officials of external audits by CROs and sponsors.  Assists the Principal Investigator in submission of accurate and timely closeout documents. ACHEIVEMENTS:  Actively Participated in the Seminar NATIONAL LEVEL SEMINAR ONTRENDS AND PERSPECTIVES IN BIOTECHNOLOGY Organized by Sri Venkateswara college of Engineering. TRAINING:  Actively Participated in the Training on GOOD CLINICAL PRACTICES at Quest Life Sciences PVT LTD, Chennai.  Actively Participated in the Training on BASIC LIFE SUPPORT TRAINING PROGRAM at Quest Life SciencesPVT LTD, Chennai.  Actively Participated in the Training on BASIC LIFE SUPPORT TRAINING PROGRAM at MEHTA HOSPITALS PVT LTD, Chennai.
  • 3. AREA OF INTEREST:  Clinical Research Associate  Clinical Trials  Clinical Data Coordinator  Clinical Data Management  Quality Control & Quality Assurance. KEYSKILLS:  Effective oral and written communication skills  Excellent interpersonal skills  Strong attention to detail  Basic computer skills and the ability to learn appropriate software  Good English language and Communication skills  Ability to work in a team or independently as required  Ability to travel and spend 60 to 80%ofworking week at site  Basic software and computer skills,including MS Office applications PERSONAL DETAILS: Fathers Name : Kirubakaran.R Date of birth : 15th December 1989 Nationality : Indian Gender : Male Marital status : Unmarried Languages known : English, Tamil & Hindi. Present Address : 2070/1, Subham Apartments, 5th Street, Nehru Nagar, 13th Main Road, Anna Nagar, Chennai-600040. Permanent Address : 2/154, Mangudi, South Street, Thirumangalam (PO), Mayiladuthurai (TK), Nagapattinam (DT)-609811. Mobile : +919677340846 & 8452866323. Email ID : kambli.k89@gmail.com DECLARATION:  I hereby declare that the above-mentioned information is correct up to my knowledge and I bear the responsibility for the correctness of the above-mentioned particulars. Date: Signature