The Veritas Healthcare Solutions is a full line Clinical Research Consulting and Site Management Organization that specializes in providing solutions to the twin challenges of speed and cost in clinical drug development. We provide cost effective solutions and full research support from Phase I to Phase IV clinical trials to the global pharmaceutical, biotechnological (or biopharmaceutical) and medical device companies.



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




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;

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
Office hours: 10.00am to 5.00pm (EST) Mon-Fri
Email:pwalia@theveritashealthcare.com
Office: (001)212-359-9474
website:www.theveritashealthcare.com