Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post : Senior Scientific Writer II
Job Description
Summary
To write, support and manage projects to prepare high quality medical and scientific communications including, literature review, abstracts, posters, slide sets, Manuscripts (sophisticated) for publication/ presentation at congresses or internal medical and/or clinical teams.
Key Responsibilities
• Prepares, literature review, abstracts, posters, and slide sets, and Manuscripts (sophisticated) working from various data sources including clinical study reports, patient profiles, protocols etc.
• Performs quality control (QC) checking / proof reading of the above mentioned deliverables to meet customer expectations.
• Handles multiple projects of up to two brands at any given time. Acquires feedback from customers and implements customer management tactics.
• Complies with and support group’s project management tool, standards, policies and initiatives.
• Follows Novartis specifications for documentation, specifically Novstyle, templates etc. Follows and supervises 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.
Candidate Profile
• Preparation of the above referenced documents meeting set quality standards and on time for submission to Health Authorities/ Clinical teams / Journals as appropriate. (i.e. staying in sync with standards e.g. CONSORT regarding publication of trial results, complying with journal formatting requirements etc).
• Timely preparation of medical and scientific documents to meet regulatory requirements, for publication of clinical trial results, to increase customer awareness of company products, and to support marketing activities
• B.Sc/M.Sc or M.Pharma/MBBS/PhD/MD Proficiency in English B.Sc./equivalent with 8 years Clinical Research (CR) experience
• M.Sc./M.Pharma +6 years of clinical research (CR) experience
• Doctoral Degree or Qualification in Medical Sciences (MBBS/MD/equivalent) PhD + 4 year of CR experience, MBBS/equivalent + 4 year of CR experience, MD +2 years of CR exp.
Additional Information
Location : Hyderabad
Business Unit : CTS
Functional Area : Research & Development
End Date : 30th October 2024
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