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| Job Location | Hyderabad |
| Education | Not Mentioned |
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| EmploymentType | Full-time |
277051BR
Scientific Writer 2Job Description
1. Prepares literature review, abstracts, posters, and slide sets working from various data sources including clinical study reports, patient profiles etc. 2. Performs quality control (QC) checking / proof reading of above documents to meet customer expectation. 3. Manages assigned individual projects. 4. Obtains feedback from customers. 5. Complies with and support group s project management tool, standards, policies and initiatives. 6. Follows Novartis specifications for documentation, specifically Novstyle, templates etc. 7. Follows and track clinical trial milestones for assigned projects. 8. Maintains records for all assigned projects including archiving. 9. Maintains audit, SOP and training compliance. 10. Performs additional tasks as assigned.
Minimum requirements
Minimum: Life-science degree or equivalent B.Sc./equivalent with 4 years Clinical Research (CR) experience, M.Sc./M.Pharm + 2 years of CR experience, Desired Doctoral degree, Qualification in Medica Good written and oral English skills Minimum: Life-science degree or equivalent B.Sc./equivalent with 4 years Clinical Research (CR) experience, M.Sc./M.Pharm + 2 years of CR experience, Desired Doctoral degree, Qualification in Medical Sciences (MBBS/MD/equivalent) PhD + 1 year of CR experience, MBBS/equivalent + 1 year of CR experience
Division
NBS
Business Unit
PLS NBS
Country
India
Work Location
Hyderabad, AP
,Keyskills :
agile communicationskills compliance copyediting proofreading ts qualitycontrol clinicalresearch projectmanagement clinicalstudy clinicaltrial ap sop pls proof medical english control dvis studyrep