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[QUOTE=Guest-IJT;109639][b]Name [/b]: Narendra K singhal [b]Email [/b]: narendrasinghal007 AT gmail.com [b]Designation / Skillset[/b] : clinical research coordinator To, Recruitment Manager Dear Sir/Mam, Sub.- Applying for CRC This is to inform you that I am Physiotherapy graduate and interested to work with your company in clinical research operations/ clinical research coordinator position. I have Two years and 4 months experience as clinical research department, lead clinical research coordinator and have strong motivation strong leadership, good communication ability good personality skill. I will be a willing to implement my full potential skills to bring benefit for your company. For your further information. I enclose my curriculum vitae. Hope my application will receive your favorable consideration and that you will give me an opportunity of interview. I would appreciate your decision very much and I look forward to hearing good news from you. Thank you so much for your kind attention. Dr.Narendra K Singhal [u][b]Resume[/b][/u] : CURRICULUM VITAE Career Objective To be a successful Professional in Clinical Research & Physical therapy. To be able to scale new heights, by taking up challenging assignments that can be fully exploit my talent in the domain of Clinical studies, simultaneously symbiotically enriching ‘self-worth’ and growing with the organization. Work Experience Have an overall total experience of Two years and 4 Months in Physical therapy stream and Two year and 2 months as Clinical Research Coordinator at clinical Research Department, (Primary and back-up coordinator) with experience for 6 Global/ multi-national studies (Phase III) for therapeutic area like Endocrinology and Consultant Physiotherapist at Diabetic clinic. [b](A)Current Position [/b]:- [b](1) Working site Name [/b]: Diabetes Thyroid & Endocrine Centre, Jaipur. [b]Designation [/b]: Clinical Research Coordinator [b]Duration [/b]: 05/Mar/ 2009 to till date Job-Responsibilities - Working in coordination with Principal Investigator and study team to conduct trial in accordance with protocol, ICH GCP and regulatory requirement. - Collate ethics committee documents/facilitate EC submission according to EC SOP. - Fill the feasibility Questionnaire and send the required documents to the CRO for the perusal. - Maintain and Update site file in accordance with GCP and Sponsors SOP. - Provide update on patient recruitment PI, Sponsor and CRO.. - Conducting the patient visits and make efforts for retention of patient. - Monitored all source documents, Lab reports, Medical records and all study related records before transcribe eCRF and CRO monitoring. - Facilitate monitoring visit and prepare the required documents for monitoring visit. - Make documents available for monitoring visit. - Case Report Form (both eCRF and Paper CRF) completion according to the CRF completion Guidelines. - Scheduling & Organizing Patient’s follow up visits. - Maintain communication between the sponsor, site and ethics committee. - Monitored Completion of source documentation (ICF and all the study visit) - Resolution of DCF - Resolution of queries - Acknowledge receipt of IP and keep them in appropriate environment. - Maintaining the entire study related activity like assist PI for consenting, Complete requisition form for blood samples, IVRS, drug dispensing, arrange logistics etc. - Coordinating with CRA/CTL/PM of CRO. - Checking of Study Inventory - Completing of action item for the site monitoring visit and audits. [b](2) Hospital Name [/b]: Diabetes, Thyroid and Endocrine Centre 11, Shivaji nagar, Civil Lines, Jaipur. [b]Designation [/b]: Consultant Physiotherapist [b]Duration [/b]: 01/Jan/2009 to Till Date Job-Responsibilities - Assist OPD with Senior Doctors (Mainly Patient with indication of Diabetes Mellitus Type-2, Neuropathy and obesity disease. - Took vital signs of patient - Took explain past and current history of patient. - Plan exercise for the diagnostic conditions. - Manage diagnosis of disease with help of Investigations & Medical Report - Assist Principal Investigator to evaluate inclusion / exclusion criteria for clinical trials undergoing in the clinic, [b](B) Previous Positions [/b]:- [b](1) Hospital Name [/b]: SAIMS,Indore (MP) [b]Designation [/b]: Assistant Trainee Physiotherapist [b]Duration [/b]: 04/Apr/2008 to 20/ Dec/2009 Training / Conferences / Seminars Participated - Attend workshop in investigator meetings about to reporting safety event, Pregnancy events,SUSAR . - Attend GCP training from Novo Nordisk in July 2009. - Attend GCP training from different sponsors in Investigator meeting in India and Abroad. - Attend Protocol Training, lab handling training, ERT(E.C.G.)training, Different type of equipments training (INR device, BNP and Pro BNP device, CGM, Use of Glucometer, Omron B.P. instrument) in 6 National and Inter National Investigator Meetings. Computer skills - I am having a good working and programming knowledge in Microsoft Excel, Word, Power Point, and Accessing Internet for Research collection data and done certificate course of Basic computer knowledge in 2000. Educational and Industry experience summary (1)I have completed my studies, B.P.T. in year 2008 and joined Shree Aurobindo Institute of Medical Sciences, Indore (MP) as Assistant Trainee Physiotherapist after One year decided to continue my career in Clinical Research. (2)In month of Jan 2009 I got an opportunity to Join Diabetes, Thyroid & Endocrine Centre,Jaipur as Consultant Physiotherapist, where I have started my clinical research career as Clinical research Coordinator in Month of 05/Mar/2009. And assist OPD with Senior Doctors to improved clinical aspects preferably help in clinical trial projects. Since Aug 2010, I achieved the position of Lead Clinical research Co-Ordinator in the Dept. of Clinical research, Diabetes, Thyroid & Endocrine Centre.. Name and Location of Institution Degree and Year Awarded Area of Study N.I.M.T. College of Physiotherapy, Jaipur Rajasthan(JRN Rajasthan Veedhyapeeth University,Udaipur,Rajasthan) B.P.T. 2008 With 70% Bachelor of Physiotherapy Sardar Senior Secondary School, Kotputli, Jaipur XII, 2000 with 54% (Chemistry, Physics, Biology) Strengths - Analytical abilities, Quick Grasping Power and Zeal for learning new things. - Ability to work as a good team member as well as independently. - Time conscious and result oriented. - Handling and working Knowledge of different Global central labs involve in clinical trials-Quintiles, BARC, MDS, Religare. - Handling and working Knowledge of different eCRF involve in clinical trials like inform (Version4.6 and other versions, RDC oracle, EDC portal) and also working in paper CRF. - Handling and working Knowledge of different IVRS/IXRS involve in clinical trials-Like Almac, ICO-Phone, Clin- Phone, Perceptive, UBC, Bilcare. [b]Other Details [/b]:- Notice Period- 1 Month Preferred Location- Gurgaon/Delhi/Jaipur/Bangluru/Mumbai Present Working Address- Diabetes, Thyroid and Endocrine Centre 11, Shivaji nagar, Civil Lines, Jaipur (Rajasthan). References Add on request [Narendra K Singhal] Date- 05/Jun/2011 ------------------------------------------------------- [b]More Information about this submission and submitter [/b]:- ___________________________________________________ [b]Submission ID [/b]: 4213416 [b]Date & Time [/b]: 5th Jun 2011 11:40 AM (UTC) [b]IP Address [/b]: 27.60.68.219 [b]Browser Info [/b]: Mozilla/4.0 (compatible; MSIE 7.0; Windows NT 5.1; .NET CLR 2.0.50727; .NET CLR 3.0.04506.30) Predicted Country : --[/QUOTE]
