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[QUOTE=Guest;226537]Hello 
I would like to apply for clinical research/ clinical research coordiantor post in your esteemed company.please find my resume 
[b]Name  [/b]: Jonaki Roy
email -jnkroy AT yahoo.com 
objective
To be a part of an organization that is innovative and continuously strives for improvement in projects and processes. One in which I can contribute my knowledge and skills for the growth of an organization and to be able to implement solutions that meet the customer requirements using my technical expertise and domain knowledge.
[b]Clinical trial and data Management Knowledge [/b]:
- CRF Designing, Database designing, Database Testing (User Acceptance Test), Edit Check Specification, Writing language, Edit Check Testing, Data entry, Data Validation, Database Quality Control.
- Knowledge on Medical Coding and 21 CFR Part 11.
- Aware of Data Validation procedures and database Closure.
- Ability of Query Resolution. 
- Aware of CDISC , CDASH and Q.A., Q.C. In CDM.
- Clinical trial management with site monitoring, site feasibility, PI selection, source document verifications, Adverse event reporting, Drug shipment and accountability , timely site coordination ,training to site personnel for protocol, study plan, CRF entry, maintaining and updating TMF, etc. 
- The Principles of ICH-GCP Guidelines, Schedule – Y.
- Bioequivalence/Bioavailability studies in Drug Development process.
job experince 
Clinical Trial Coordinator. 
Worked as CRC in Risk Care & Prakruti Hospital for Clinisearch CRO Thane.
[b]Role and Responsibilities [/b]: As a Clinical trial Coordinator.(Oct 2011-dec2011)
- Collecting history of the patient and performing appropriate screening according 
to the inclusion/exclusion criteria.
- Followed ICF procedure during patient recruitment for study.
- Ability for query resolution & DCF resolution. 
- Observation of Subject during follow up visits with .
- AE/SAE documentation & reporting while conducting study .
- Coordinate trial related activities with the CRA. 
- Coordinate with the patients & doctor for trial related activities.
- Maintaining Site Master File ,drug accountability log, Source documents and IP storage in hospitals
- Assignment includes ethics Committee Approval, Screening, Recruiting, Monitoring visits of Patients,, Monitoring SAE’s and AE’s.
[b]Active Participation in below Studies as CRC  [/b]: 
- A Multicentric, randomized, open label,,prospective two arm , comparative study in treatment of lower respiratory tract infection.
- A multicentric, randomized,open label, comparative study to evaluate the safety and efficacy in treatment of type II diabetes
- Convergys Corporation Thane
As Senior Customer Care Officer Aug 2008- Apr 2009
- Spryance India(Transcend) Pune
As Home-Based Medical Transcriptionist Mar 2007 –Aug 2008
 And as Proof Reader Aug 2010 Feb 2011.
- Reliance Info Streams Pvt Ltd. Navi Mumbai
As Customer Care Representative Dec 2003-June 2005
Educational Qualification
Year passed
 Degree/Dipl Subjects % School/College
1998 SSC Sci, Maths, Eng, French Hindi 73 % KHS pune
1990 HSC Science, Maths 56 % Fergusson College Pune
1995 Bsc Bot,Geo,biochemChemistry(main) 59 % Pune University.
2007
 Diploma in MT Medical Transcription 82% Spryance Pune
2010-2011
April 2012 Post graduation in clinical & Data mngt
Pursing Certification for CRA Clinical research &
Clinical data management
 67 % ICRI Mumbai
Veritas Healthcare Solutions New York[/QUOTE]

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