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[QUOTE=Guest;112061]Veeranna S S
 [b]E-mail [/b]: Veeranna.ss AT gmail.com 
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[b]Career objective [/b]: Looking for challenging career in organization which would best utilize my skills and would provide me an opportunity to grow personally and acquire knowledge in my field by putting me on challenging assignments. 
[b]PROFESSIONAL EXPERIENCE [/b]:
[b]1) Organisation [/b]: Infosys
[b]Duration [/b]: 34 months (11-Jun-2007 to 1 April-2010)
 [b]Position [/b]: Senior Process Executive
[b]2) Organisation [/b]: Lotus Labs
[b]Duration [/b]: 6 months (Internship) from 18 June 2010 to 22 Dec 2010.
[b]Position [/b]: Clinical Research Co-ordinator (Nasik, Maharashtra)
[b]3) Hospital [/b]: Raga’s Skin care
[b]DOJ [/b]: 1 April 2011 till the date.
[b]Position [/b]: Clinical Research Co-ordinator
[b]Project experience [/b]:
[b]Protocol Title [/b]: A Multicenter, Double-Blind, Randomized, Vehicle-Controlled, Parallel-Group Study Comparing -------------------- In the Treatment of Mild to Severe Acne Vulgaris.
- Started the project from Site initiation level.
- Coordinating with Ethics committee regarding submission of Protocol, amended Protocol, SAE, deviation and other study related reports. 
- Writing source documents (20 patients, 5 visits).
- Communicating with patients for their follow up.
- Hands on experience on E-CRF filling.
- Have good experience in handling E-CRF (updated 20 patients, 5 visits details)
- Providing Randomised IP’s to the patients. 
- Maintaining logs and forms (IP log, Temp log, Randomisation log, patients visit tracking log, Screening log, enrolment log, etc)
- Updating and maintaining ISF and co-ordinating with CRA to update and maintain CSF.
- Experience of working under strict timeliness, meeting sponsor SLA. 
[b]Rewards [/b]:
- Got progression as senior process executive on 1 December 2008.
- Completed six sigma (Yellow belt) training on November 2008.
- Lead the first six sigma (Yellow belt) project and completed on September 2009 with soft savings of $1875USD.
- Got RAMP award for good performance.
- Received SPOT award for good performance and providing various process improvement ideas.
- Awarded with both Client and Infosys award for the best Team Player.
[b]Additional Responsibilities [/b]:
- Reconciliation of daily activities.
- Working on daily and weekly client reports.
- Documentation of employees’ details in SAP.
- Handling Team meetings and organising Team building activities.
- Reviewing study Case Report Forms (CRFs) completed by the sites, and verifying entries by validating accurate source documentation to support CRF entries. 
- Documenting site visits and issues in reports and follow-up letters to the site.
EDUCATIONAL CREDENTIALS
- A graduation in B.SC with Bio-technology, chemistry, and zoology has main subjects and has secured 84 % marks 2007 batch (Kuvempu university)
- PG-Diploma in Clinical Research from LCRA 2011 batch (LCRA).
(Knowledge on ICH-GCP, Indian GCP, Ethics committee, Regulatory bodies, ICMR guidelines, CDER, CBER, FDA guidelines, EU directives, 21 CFR part 11, part 50, part 54, 56, 312 and 314, SOP, Protocol, CRF, ICF, ISF, BA-BE studies, Clinical trial designs, Investigator meetings, EC submissions, site monitoring, clinical study reports, site close-out reports)
- Knowledge about Clinical Analytics 4.0[/QUOTE]

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