They pride ourselves on their ability to provide innovative quality solutions to meet clinical challenges, all delivered RIGHT ON TIME….EVERY TIME.
Their industry-standard, validated SAS and data management system, compliant with ICH GCP guidelines and 21 CFR Part 11 regulations is a guarantee that you will always be provided with data of the highest quality.
Post: QA Specialist/ SOP Writer- CRO
Job Description:
Write & Manage & Compose SOPs for DM, Biostats and Clinical Research as per 21CFRPart11
Create and Modify existing Quality Systems
Serves as clinical QA representative on clinical project teams, conducts internal and external CQA audits
Candidate Profile:
Documents audit observations; evaluates impact, and makes recommendations for corrective actions.
Bachelor’s degree with 1-3 years relevant experience in CRO industry;
Excellent documentation skills.
Additional Information:
Experience: 1-3 Years
Location: Delhi
Education: B.Pharm, M.Pham, B.Sc, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR, QA
End Date: 18th August, 2011
Submit your resume at, hire@tech-observer.com
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