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[QUOTE=Guest-IJT;110682][b]Name [/b]: chaithanya [b]Email [/b]: chaitanya.valleti3 AT gmail.com [b]Designation / Skillset[/b] : clinicalresearch co-ordinator Dear Dr.Sir, I am Chaithanya.V, a graduate student (B-pharmacy) with a specialization in clinical research from the ICBio, Hyderabad, INDIA. My interest lies in the fields of clinical research data management and it’s allied fields which involves CRF design, eCRF design, edit checks, data validation, quality of the data. In view of my interests and background, coupled with my expertise in quality control and great enthusiasm to learn new techniques, I wish to pursue my career in your organization. I would be very great ful to you, if you could shed some more light on the job description on the position available. Further, I would like to request your good self to consider my application for a vacancy in your organization and do the needful. I am also attaching my CV along with this letter for your perusal. Thanking You, Regards, [u][b]Resume[/b][/u] : Valleti chaithanya To progressively expose myself in the area of Clinical Research for a greater and better change and to seek a respectable position where acquired skills and knowledge can be utilized towards continuous growth in the field of clinical research and development. - Worked as a Trainee CRC with pulse (smo), hyderabad from Mar 2010 - Dec2010. - Working as a Clinical Research Coordinator with Pinnacle Clinical Research Pvt. Ltd. (SMO) Hyderabad from 21-Jan-2011 to till date. - Worked as a Clinical Research Coordinator at Keerthi neuro Care, Tirupathi from 21-Mar-2011 to till date. - P.G .Diploma course in ClinicalResearch & Clinical Data Management from Biorevelationz , Hyderabad. - Active Projects [b]- Phase III (International Trial); Indication [/b]: Migraine in Children & Adolescents with Parexel International Synchron Pvt Ltd. Doing referral activities for other sites which has least enrolled patients - Performing Site feasibility, Site Initiation, and Internal QC Visits - Reviewing Medical Records to Identify Potential subjects for the study - Assisting the PI in the ICF process, screening & enrollment - Doing the IWRS/IVRS for Randomization - SMF - Maintaining and updating the file - Completing the eCRF and Paper CRF within the timelines. - Safety - Coordinating SAE reporting on time , Drug ordering and Archiving. - Interacting with the Institution ethics committee as per the directions of the Investigator - Coordination of Monitoring & Audit visits - Organizing study team meetings at the site - Scheduling subject visits to ensure 100% subject compliance & subject retention [b]Handling of Clinical Trial Management Software [/b]: - Handling of clinical trial management application software like CRF Workflow. - Handling the e-Crf and paper CRF. [b]Regulatory and Ethical Affairs Assistance [/b]: - Monitoring of ICH-GCP, Regulatory compliance of clinical trial studies - Assist site in ethical committee application process - Document submission for Ethical/regulatory clearance. - Bachelor of pharmacy (B.Pharm) from Annamacharya College of Pharmacy, Rajampet with 64.5% (2005-2009). - Intermediate [BiPC] with 78.8% (2002-2004). - Secondary School with 82.2% (2002). - - Inform Phase Forward Version 4.5 - Inform Phase Forward Version 4.6 [b]- Tools [/b]: MS Excel, MS Word, MS Power Point [b]- Operating System [/b]: Windows2000/Xp [b]DECLARATION [/b]: I hereby declare that all the statements furnished herein are true, complete and correct to the best of my knowledge. Chaithanya.V ------------------------------------------------------- [b]More Information about this submission and submitter [/b]:- ___________________________________________________ [b]Submission ID [/b]: 4135179 [b]Date & Time [/b]: 16th May 2011 6:31 AM (UTC) [b]IP Address [/b]: 117.242.59.38 [b]Browser Info [/b]: Opera/9.80 (Windows NT 5.1; U; en) Presto/2.6.30 Version/10.63 [b]Predicted Country [/b]: India[/QUOTE]
