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[QUOTE=Guest-IJT;112349][b]Name [/b]: libin [b]Email [/b]: libinalappatt AT yahoo.com [b]Designation / Skillset[/b] : Clinical Research Coordinator/ Team Leader Sir, I would like to introduce myself as Libin Jose. I have completed my Masters in Biotechnology and have completed a post graduate Diploma in Clinical Research. I possess an experience of Three year and three month as a Clinical Research Coordinator.Presently I am working as Clinical Research Team Leader at Epsilon Clinical Research Pvt.Lmt. I have my residential in India but I will ready to relocate to any where. To further acquaint with my Profile and educational background, I have attached my resume for your perusal. Thank and Regards Libin Jose [u][b]Resume[/b][/u] : OBJECTIVES A position in Clinical Research in the medical field while merging into a globally focused organization that will purposefully utilize my qualifications and Experience while offering several opportunities to integrate personal enrichment with professional goals. ACADEMIC QUALIFICATIONS MSc Biotechnology Bharathidasan university First Class BSc Biotechnology Bharathidasan University First Class PG Diploma in Clinical Research Sysplex Bioclinical Solution COMPUTER SKILLS - MS WORD, - MS EXCEL - Internet and E-mail Previous Experience 1. Omega Hospital Mangalore [b]Designation [/b]: Clinical Research Coordinator [b]From [/b]: Feb 2008 to March 2010 CURRENTLY WORKING 2) EPSILON CLINICAL RESEARCH PVT.LMT [b]Designation [/b]: Clinical Research Team Leader/ Study coordinator April 2010 to till Date TOTAL YEARS OF EXPERIENCE 3 year and 3 Months CLINICAL TRIALS HANDLED PHASE INDICATION DESIGNATION STATUS II ACS CRC COMPLETED II PAH CRC COMPLETED II PAO CRC ON GOING III AF CRC ON GOING II ACS TEAM LEADER ON GOING III ACS TEAM LEADER ON GOING III ACS TEAM LEADER ON GOING III DM TEAM LEADER ON GOING [b]PRESENT WORKING PROFILE [/b]: - Monitoring in the compilation of the study related documents during the pre trial Period - Ensuring the conduct of the trials as per the ICH GCP & Protocol Specified guidelines - Assisting study managers for startup activities & site initiation - Site Initiation - Assist in the process of IVRS - Recruitment & Retention - Assist in the process of administering the informed consent to potential patients and discussing in detail the patient information sheet - Follow up with site team for timely completion of the Source Documents and ensuring that all the relevant information required in the Case Record Form are present in the source document - Complete the Case Record Forms within the timelines and with minimal errors - Schedule subject visits as per the protocol to ensure maximal subject compliance retention - Coordinate all lab related activities – shipment of samples through the designated courier and ensure timely receipt of the lab reports - Compile and update the Trial Master File - Maintain the study related logs – screening, enrolment, drug administration, temperature and other communication logs - Manage the accountability of the Clinical Trial Material - Coordinating Ethics Committee Submission & Approval - Coordinate for any query from the Ethics Committee - Feasibility Data from various Investigators - Conducting trial specific feasibilities, Collecting Interacting with Site/PIs & other study member on regular basis, discuss potential issues and suggest corrective action LANGUAGES KNOWN [b]Speak [/b]: English, Malayalam,Hindi, Tamil and Kannada [b]Write [/b]: English, Hindi, Malayalam [b]Read [/b]: English, Hindi, Malayalam REFERENCE Dr.Kasim A.K CEO Epsilon Clinical Research Mangalore Heart Scan Foundation, Kumar’s International, Opp. Colaco Hospital, Bendoorwel, Mangalore - 575 002 Mr. Satyabrata Dash Operational Manager Epsilon Clinical Research Mangalore Heart Scan Foundation, Kumar’s International, Opp. Colaco Hospital, Bendoorwel, Mangalore - 575 002 DECLARATION I hereby declare that the information provided above is true to the best of my knowledge. [b]Place [/b]: [b]Date [/b]: LIBIN JOSE ------------------------------------------------------- [b]More Information about this submission and submitter [/b]:- ___________________________________________________ [b]Submission ID [/b]: 4206837 [b]Date & Time [/b]: 3rd Jun 2011 10:35 AM (UTC) [b]IP Address [/b]: 122.167.40.183 [b]Browser Info [/b]: Mozilla/5.0 (Windows NT 5.1) AppleWebKit/534.24 (KHTML, like Gecko) Chrome/11.0.696.71 Safari/534.24 Predicted Country : India[/QUOTE]
