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[QUOTE=Guest-IJT;152310][b]Name [/b]: Amruta
[b]Email [/b]: amruta.kudale AT rediffmail.com
[b]Designation / Skillset[/b] : Clinical research asssociate or coordinator

[u][b]Resume[/b][/u] :
 
OBJECTIVE To work in challenging job environment that utilizes my skills and ability, and offer ample learning opportunities. 
ACADEMIC
PROFILE B. Sc (Microbiology) 2005 First Class
Pune University
P.G. in Clinical Research 2007 First Class
PREVIOUS WORK EXPERIENCE
[b]1) Company name [/b]: eClerx Services Limited, Hinjewadi, Pune
 [b]Designation [/b]: Analyst
 [b]Duration [/b]: 26th February 2009 to 12th January 2011
[b]Job Responsibilities [/b]:
- Trades drafting , reconciliation
- Data management
- Managing team activities and work
- Reporting to client using spreadsheet
- Achievement of targets with exact Q&Q as per client requirements
- Training to New Joiners on Process & financial products
- Preparation of SOP’s for process
- Client communication on daily issues, requirements, process update
[b]2) Company name [/b]: Orange Life sciences, Tilak Road, Pune
 [b]Designation [/b]: Trainer for Clinical research
 [b]Duration  [/b]: 01 March 2008 till 15 February 2009
[b]Job Responsibilities [/b]:
- Conducting seminars for Clinical research awareness throughout Maharashtra
- Student counseling with respect to clinical research
- Training to clinical research students for full time & part time availability on topics mentioned below
- Overview of Clinical Research
- Pharmacology & BA BE Studies
- Drug Development
- Biostatistics
- Codes and Oaths
- Regulatory Compliances
- Schedule Y
- Design of Trials
- Finance Management
- Management of Trials
- Clinical Data Management
- Adverse Event Reporting
- Clinical trial monitoring & auditing
[b]3) Company name [/b]: Centre for Rheumatic Diseases, C/o. ARCF Foundation, Pune Camp 
 [b]Designation [/b]: Trainer for Clinical research
 [b]Duration  [/b]: 01 March 2008 till 15 February 2009
[b]Job Responsibilities [/b]:
- Working as a paramedic for referral practice patients.
- Includes filling of patient’s information sheet.
- Data entry of respective information in custom built software.
- Promoted as Sr.Field Asst. for a Rural Population study based on spread viral disease with reference to persistent ‘Rheumatic Musculoskeletal Disorders’.
- Carrying out the trials at clinic using GCP (Good clinical practice) under supervision of PI (principal investigator).
- Studying the site, enrolling the participants for trial, follow –ups, maintaining, dispensing drugs, performing the experiments, taking the projects to completion, testing the accuracy, creating the reports as well as regulatory documents adhering to the CPG (clinical practices guidelines) under guidance of PI and ethics committee.
- Coordinate with prime investigators, departments, central administration, personnel, financial, support, and guidance departments of the clinical research centers.
- Managing team work on field
- Managing patient’s visits, classifying treatments protocols and maintaining checkups with
COMPUTER SKILLS
 Short term Course of Information technology (MS-CIT) with first class
Hands on knowledge of MS-Office
 
 
ADDITIONAL INFORMATION I am an individual who values discipline and commitment. I have been successful in adapting the varying demands of different situations. My inquisitive nature towards work has always helped me to become a thorough professional.
My commitment to tasks has always benefited me in delivering my best.
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[b]More Information about this submission and submitter [/b]:-
___________________________________________________
[b]Submission ID  [/b]: 4456723
[b]Date & Time  [/b]: 8th Aug 2011 5:26 AM (UTC)
[b]IP Address  [/b]: 117.195.64.113
[b]Browser Info  [/b]: Mozilla/5.0 (Windows; U; Windows NT 5.1; en-US; rv:1.9.2.18) Gecko/20110614 Firefox/3.6.18
Predicted Country : India[/QUOTE]

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