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[QUOTE=Guest;160825]Malli Janki R. [B]Email [/B]:- jankiamrutia AT yahoo.co.in [B] Career Objective [/B]: Keenly interested in challenging and resourceful assignment, which will enable me to sharpen up my skill and make me competent enough to excel in my field. Utilizing knowledge, ideas and experience for producing best result in order to achieve prime goal of the institution or organization. [B] Assets [/B]: - Strong determination, self-belief and will power. Decision Maker, Fast learner - Proactive and positive attitude. - Inquisitive with time management skills and leadership charisma. - Good communication, presentation skills. [B] Academic Qualifications [/B]: M.Pharm (P’Cology)-NGSM Institute of Pharmaceutical Sciences (Mangalore), under Rajiv Gandhi University of Health Sciences (Bangalore), 2008-2010-78.82%, Distinction B.Pharm-NGSM Institute of Pharmaceutical Sciences (Mangalore), under Rajiv Gandhi University of Health Sciences (Bangalore), 2003-2007-74.04%, Distinction Class XII G.T. Sheth, High School, Rajkot, 2003-54% 2nd class Class X S.N.Kansagra School (ICSE), Rajkot, 2001-79%Distinction [B] Dissertation Topic (At PG Level) [/B]: “EFFECT OF SOME DOPAMINERGIC ANTAGONISTS ON ALCOHOL DEPENDENCE AND ALCOHOL WITHDRAWAL IN RATS AND MICE’’. [B]WORK EXPERIENCE :[/B] Synchron Research Services Pvt. Ltd., Ahmedabad. Officer in Biometrics and Data Management (March 15, 2010 till date). [B]Roles and Responsibilities [/B]: - Preparation of synopsis for BA/BE and Clinical Trials. - Designing of Protocols and ICF for BA/BE and Clinical trails (Phase I to IV) in coordination with other departments. - Preparation of meal plan in accordance with standardized menu provided by the dietician - Design and preparation of Case Record Forms for BA/BE and Clinical trials (Phase I and IV). - Medical coding of adverse events using MeDRA® SOFTWARE. - Coding of concomitant medication using WHO Dictionary. - Review of listings and incase of discrepancy, request for the generation of DCF to the Data Associate. - Interpreting the results of Clinical Trails (Phase I to IV and BA/BE). - Preparation of Final Clinical Study Report for BA/BE and Clinical trials. - Dispatch of Final Clinical Study Report to sponsor. - SOPs (applicable to the department) preparation and updating. - Implementing the recommendations according to the latest guidelines. - Preparation feasibility questioners, interact with potential investigators for study feasibility. - Recruitment rate and protocol inputs. [B] Computer Awareness [/B]: - Familiar with MeDRA® coding and WHO dictionary - Internet skills - MS-Office. [B]Seminars attended :[/B] - National level technical symposium on Novel concepts in pharmaceutical research, NGSMIPS, Mangalore. - Regional seminar on qualitative research methodology and regulatory affairs, NGSMIPS, Mangalore. - Screening of Drugs acting on CNS, KMC, Manipal. - Attended IPC,2009, Ahmedabad[/QUOTE]