Job Description:
- Process serious adverse event cases and other medically related information
- Review safety tracking systems for accuracy and quality
- Perform review of clinical data (case report forms)
- Review CRF/eCRF data completeness, accuracy and consistency via computerized edits and manual data checks
- Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets
- Create data set specifications
- Validate data sets per the formal, documented process
- Create data programming specifications per specified study requirements
- Create and validate clinical data programs
- Qualification: B.Sc./M.Sc. Biotechnology
- Experience: 0-1 years
- General computer literacy
- Knowledge of database technologies and processes
How to Apply:
Interested candidates can directly Walk-In for the Interview.
P.N. Confirm your arrival by sending a mail at info@hysynth.com
Walk-In Details:
Date: 12th May - 17th May, 2014
Time: 10 AM - 5 PM
Venue: HySynth BioTechnologies Pvt. Ltd., Robert V Chandran Towers, 5th Floor, #149, Velachery - Tambaram Main Road, (Near Velachery Railway Station and Doshi Apartment) Pallikaranai, Chennai - 600 100, Tamilnadu, India.
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