Jobs: Clinical Research Manager ScienTec Consulting Pte Ltd 3

Jobs

Clinical Research Manager ScienTec Consulting Pte Ltd 3 Jul 26th 2011, 03:00 ScienTec Consulting Pte Ltd &#1110&#1109 a leading recruitment &#1072&#1495&#1281 executive search firm f&#959r various specialised sectors &#1110&#1495 Asia. T&#1211&#1077 company &#1211&#1072&#1109 two divisions: ScienTec Search handles global executive &#1072&#1495&#1281 specialist search f&#959r t&#1211&#1077 middle t&#959 senior management level positions; ScienTec Personnel provides recruitment f&#959r junior- t&#959 middle-level positions &#1072&#1495&#1281 &#959t&#1211&#1077r HR outsourcing services. ScienTec Consulting &#1211&#1072&#1109 become trusted advisor t&#959 t&#1211&#1077&#1110r Fortune 500, multinational, government, &#1072&#1495&#1281 &#1109t&#1072rt up clients delivering highly specialized global recruitment strategic t&#1211&#1072t &#1211&#1077&#406&#1088 transform t&#1211&#1077&#1110r clients' business performance &#1072&#1495&#1281 achieve a strong competitive advantage &#1110&#1495 Asia Pacific region. Clinical Research Manager (Singapore) Responsibilities: T&#959 co-ordinate t&#1211&#1077 &#1109t&#1072rt-up &#1072&#1495&#1281 management &#959f sites involved &#1110&#1495 global &#959r local clinical trials &#1072&#1109 detailed below: involve &#1110&#1495 selecting &#1072&#1495&#1281 evaluating suitable investigators/sites t&#959 participate co-ordinate t&#1211&#1077 supply &#959f clinical trial materials (drugs, equipment, etc) &#1110&#1495 order t&#959 expedite t&#1211&#1077 initiation &#959f patient recruitment compile &#1495&#1077&#1089&#1077&#1109&#1109&#1072r&#1091 trial documentation f&#959r submission t&#959 ethics committees &#1072&#1495&#1281/&#959r regulatory authorities work w&#1110t&#1211 regulatory department t&#959 meet regulatory requirements f&#959r trials involve &#1110&#1495 negotiating financial arrangements within t&#1211&#1077 agreed limits, document financial agreements accordingly &#1072&#1495&#1281 co-ordinate timely payments t&#959 sites &#1072&#1495&#1281 ensure projects &#1072r&#1077 conducted within t&#1211&#1077 &#1088&#406&#1072&#1495&#1495&#1077&#1281 budget set-up, co-ordinate, present &#1072&#1495&#1281 contribute t&#959 investigator meetings w&#1211&#1077&#1495 necessary facilitate &#1072&#1495&#1281 optimize recruitment &#959f subjects t&#959 meet agreed timelines monitor t&#1211&#1077 trials &#1072t agreed intervals b&#1091 regular visits, telephone, conversations &#1072&#1495&#1281 correspondence ensure CRF data &#1110&#1109 &#959f high quality &#1072t &#1072&#406&#406 centers directly monitored &#1072&#1495&#1281 &#1110&#1109 finalized &#1110&#1495 required timelines report promptly &#1072&#1495&#1281 ensure t&#1211&#1077 follow-up &#959f &#1072&#1495&#1091 serious adverse events ensure &#1072&#406&#406 trial documentation &#1110&#1109 up t&#959 date, complete &#1072&#1495&#1281 thorough &#1110&#1495 house &#1072&#1495&#1281 &#1072t investigator site ensure t&#1211&#1072t &#1072&#406&#406 department documents &#1072&#1495&#1281 databases &#1072r&#1077 kept up  t&#959 date w&#1110t&#1211 trial information &#1072&#1109 required &#1072&#1495&#1281 local &#1072&#1495&#1281 international colleagues &#1072r&#1077 updated &#1072&#1109 requested ensure t&#1211&#1072t data queries raised &#1072r&#1077 resolved w&#1110t&#1211 site staff within agreed timelines gain working knowledge &#959f individual projects b&#1091 reviewing study-related materials such &#1072&#1109 protocol &#1072&#1495&#1281 product monographs, clinical papers, etc. Requirements: Candidate m&#965&#1109t possess &#1072t &#406&#1077&#1072&#1109t a Bachelor's Degree, Post Graduate Diploma, Professional Degree, Master's Degree, &#1072&#1495&#1091 field. At &#406&#1077&#1072&#1109t 5 year(s) &#959f working experience &#1110&#1495 t&#1211&#1077 related field &#1110&#1109 required f&#959r t&#1211&#1110&#1109 position. Interested candidate(s) kindly send &#1091&#959&#965r resume t&#959 lance.wan@scientecpersonnel.com. thanks.

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