Work activities include:
Developing and writing trial protocols (outlining the purpose and methodology of a trial);
Designing data collection forms, known as case record forms (CRFs);
Coordinating with the ethics committee, which safeguards the rights, safety and wellbeing of all trial subjects;
Managing regulatory authority applications and approvals that oversee the research and marketing of new and existing drugs;
Liaising with doctors/consultants (or investigators) on conducting the trial;
Setting up the study centres, which includes ensuring each centre has the trial materials and training site staff to trial-specific industry standards;
Verifying that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV);
Collecting completed CRFs from hospitals and general practices;
Writing visit reports;
Closing down study centers on completion of the trial;
Discussing results with a medical statistician, who usually writes technical trial reports;
Archiving study documentation and correspondence;
Qualification:
UG - B.Pharma - Pharmacy,B.Sc - Any Specialization,MBBS - Medicine
PG - M.Pharma - Pharmacy,M.Sc - Any Specialization,MBA/PGDM - Any Specialization,M.S/M.D - Any Specialization, PG Diploma - Any Specialization
• Location: New Jersey and New York
Special Note:
• SOP training mandatory before placement
• H1B sponsorship for international candidates who are eligible
The Veritas Healthcare Solution.
469 7th Avenue, New York, NY -10018
Phone -212-359-9474
Web :
www.theveritasheathcare.com Email-
info@theveritashealthcare.com Office hours: 10.00am to 5.00pm Mon-Fri
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Topic: H E L P WA N T E D !!! (Read 10878 times)