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Expert Scientific Writer

8.00 to 13.00 Years   Hyderabad   25 Oct, 2019
Job LocationHyderabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryMedical / Healthcare
Functional AreaSales / BD
EmploymentTypeFull-time

Job Description

  • Prepares literature review, abstracts, posters, and slide sets, Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc.
  • Performs quality control (QC) checking / proof reading of the above mentioned documents to meet customer expectations.
  • Manages multiple projects across multiple brands at any given time.
  • Obtains feedback from customers; defines and implements customer management tactics.
  • Supports people and performance management.
  • Supports process improvement initiatives.
  • Complies with and support group s project management tool, standards, policies and initiatives.
  • Follows Novartis specifications for documentation, specifically Novstyle, templates etc.
  • Follows and track clinical trial milestones for assigned projects.
  • Maintains records for all assigned projects including archiving.
  • Maintains audit, SOP and training compliance.
  • Trains new joiners, fellow colleagues as and when required.
  • Performs additional tasks as assigned.

Minimum requirements

  • Minimum: Minimum science degree/equiv. B.Sc./equivalent +10 y Clin Res experience, M.Sc./M.Pharm +8 y clin res exp.
  • Desired: PhD + 6y of CR exp, MBBS/equivalent + 6y of CR exp, MD +4y CR experience
  • Excellent written and oral English
  • Minimum: Minimum science degree/equiv. B.Sc./equivalent +10 y Clin Res experience, M.Sc./M.Pharm +8 y clin res exp.
  • Desired:PhD + 6y of CR exp, MBBS/equivalent + 6y of CR exp, MD +4y CR experience
,

Keyskills :
advisoryagile communication skillscompliance copy editingproof reading study reportsquality control

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