Vinoth Kambli's curriculum vitae summarizes his experience and qualifications. He has 2 years of experience as a Clinical Research Associate and seeks a career in a progressive environment where he can utilize his skills. He has a B.Tech in Biotechnology and diploma in Chemical Engineering. His experience includes ensuring clinical trials are conducted according to regulations and preparing documentation. He also has skills in communication, attention to detail, and working independently or in a team.
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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