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[QUOTE=Guest-IJT;125347][b]Name [/b]: Hiti [b]Email [/b]: hiti.biotech AT gmail.com [b]Designation / Skillset[/b] : Clinical research cordinator Biotechnolgist [u][b]Resume[/b][/u] : [b]CAREER OBJECTIVE [/b]: To become a successful research professional who satisfy the need of an organization where I can utilize and improve my skill and knowledge efficiently, while being resourceful, innovative and flexible. [b]EDUCATIONAL PROFILE [/b]: - PDCR (Professional Diploma in Clinical Research) from catalyst clinical service Pvt.Ltd. Delhi. - M.Sc. Biotechnology with 71% from International College for Girls, Jaipur, Rajasthan, India. - B.Sc. Biotechnology with 72% from M.J.R.P Mahila Mahavidhyalaya, Jaipur, Rajasthan, India. - Senior secondary with 65.23% from V.S.S.P.School ,Phulera , Jaipur - Secondary with 64% from K.V .Phulera , Jaipur - Pursuing “Diploma in Nutrition and Health Education” from IGNOU (VMOU). [b]TRAINING AND CERTIFICATES [/b]:- - Clinical Research Assistant at Fortis Escorts Hospital, Jaipur, Rajasthan and have participated in Phase III and VI Multicentric and Multinational Clinical Studies from 25 Feb 2011 till 25 May 2011. - Certificate for completing the NIH Web-based training course “Protecting Human Research Participants” from National Institutes of Health (NIH) Office of Extramural Research. - Certificate for completing of open access GCP test with 92% marks by Pharma XM. - Certificate for completing two days program of in Pharmacovigilance in collaboration with vedaant resources and jayoti vidhyapeeth women‘s university. Work Performed and Reviewed during training - Documentation of clinical trial data, maintaining ISF (Investigator Site File). - Assisted in the ICF process, writing source notes, screening & enrollment, sample collection, packaging, sample transfer to central labs. - Assisted in subject follow up visits. - Performed the process of IVRS. - Assisted in e-CRF and paper CRF filling, and solving DCF and resolving queries. - Participated in Monitoring Process, site SIV process and site feasibility. - Managing the accountability of the Clinical Trial Material. - Schedule subject visits as per the protocol to ensure maximal subject compliance. - Assisted in making letters for notifying EC regarding safety and making approval letters. [b]DISSERTATION WORK [/b]:- The training of 2 months duration (dissertation) in microbiology on the topic “Rapid Identification of Non Tuberculous Mycobacteria (NTM) By PCR-RFLP by hsp - 65 genes.” [b]Thesis Title [/b]: Rapid Identification of Non Tuberculous Mycobacteria (NTM) By PCR-RFLP by hsp- 65 genes.” [b]Advisor [/b]: Dr .Bharti Malhotra (S.M.S. MEDICAL COLLEGE, Jaipur) A review report on “Swine flu”. [b]EXTRA CURRICULAR ACTIVITIES [/b]: Attended a “Indian Oil Corporation sponsored 6 days signature campaign on combating foeticides by awake and sure barmar” /Jaipur (15-20-Oct ) . [b]CONFERENCES ATTENDED [/b]: - UGC sponsored National Conference on “Recent trends in environmental toxicology and biotechnological approach to conserve environment” held in Jaipur. [b]COMPUTER SKILLS [/b]: - Microsoft Office - Well verse with internet. [b]LANGUAGES KNOWN [/b]: Language(s) Read Write Speak English - Hindi - Punjabi × × - ______________________________________________________________________________ [b]DECLARATION [/b]: I solemnly declare here, that all the facts mentioned above are true to the best of my knowledge. Yours Sincerely HITI ------------------------------------------------------- [b]More Information about this submission and submitter [/b]:- ___________________________________________________ [b]Submission ID [/b]: 4297823 [b]Date & Time [/b]: 25th Jun 2011 8:59 AM (UTC) [b]IP Address [/b]: 117.196.249.48 [b]Browser Info [/b]: Mozilla/5.0 (Windows NT 5.1) AppleWebKit/534.24 (KHTML, like Gecko) Chrome/11.0.696.60 Safari/534.24 Predicted Country []: India[/QUOTE]
