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Senior Scientific Writer I

3.00 to 7.00 Years   Hyderabad   15 Aug, 2019
Job LocationHyderabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryMedical / Healthcare
Functional AreaTechnical Writing
EmploymentTypeFull-time

Job Description

Senior Scientific Writer I Job Description 1. Prepares manuscripts, literature review, abstracts, posters, and slide sets working from various data sources including clinical study reports, patient profiles, protocols etc. 2. Performs quality control (QC) checking / proof reading of literature review, abstracts, posters, and slide sets to meet customer expectations. 3. Manages up to two assigned team projects at any given time. 4. Ensures getting feedback from customers and supports implementation of customer management tactics. 5. Comply with and support group s project management tool, standards, policies and initiatives. 6. Follow Novartis specifications for documentation, specifically Novstyle, templates etc. 7. Follow and track clinical trial milestones for assigned projects. 8. Maintain records for all assigned projects including archiving. 9. Maintain audit, SOP and training compliance. 10. Performs additional tasks as assigned. Minimum requirements - Minimum: Minimum science degree or equivalent, B.Sc./ equivalent with 6 years Clinical Research (CR) experi- ence, M.Sc./ M.Pharm +4 years of clinical research (CR) expe- rience - Desired Doctoral Degre Good written and oral English skills - Minimum: Minimum science degree or equivalent, B.Sc./ equivalent with 6 years Clinical Research (CR) experi- ence, M.Sc./ M.Pharm +4 years of clinical research (CR) expe- rience - Desired Doctoral Degree or Qualification in Medical Sci- ences (MBBS/ MD/ equivalent) - PhD + 2 year of CR experience, MBBS/ equivalent + 2 year of CR experience, MD +1 year of CR exp,

Keyskills :
sopagileadvisorycompliancemedicaltudyreportsclinicaltrialclinicalresearchcommunicationskillsproofreadingcustomermanagementprojectmanagementqualitycontrolclinicalstudycopyediting

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