GlaxoSmithKline Pharmaceuticals Ltd. (GSK Rx India) is one of the oldest pharmaceuticals company and employs over 5000+ people. Globally, we are a £ 27.4 billion, leading, research-based healthcare and pharmaceutical company. In India, we are one of the market leaders.
Post : Senior Scientific Writer
• Contributes to documents and activities to be included in registration files.
• Authors clinical documents following defined templates.
• Ensures the consistency and quality level of all documents that are issued.
• Actively participates in all planning, coordination and review meetings.
• Ability to work on 2-3 assignments simultaneously.
• Proactively raises and discusses concerns/ issues in an open and timely manner and within the global team at GSK Vaccines, thereby demonstrating the ability of promoting high scientific standards by pointing out obvious flaws and proposing (and advocates) alternatives.
• Works directly with diversity of roles at different levels within GSK (e.g., Clinical Research and Development Leader (CRDL), Project Level CRDL, Regional Medical Directors and Advisors, Study Delivery Leads (SDL), Study Data Managers (SDM), Biostatisticians, other Scientific Writers).
• Establishes network of communication and continuously builds collaboration to facilitate smooth partnerships and interfaces between all groups involved in delivery of writing assignments.
Candidate Profile : 6+ years of experience in Regulatory Writing and ICH Guideline. M.Pharm / Freshers with Ph.D degree can also be considered.
Experience : 6+ years
Qualification : M.Pharm / Freshers with Ph.D degree
Location : Karnataka - Bangalore
Industry Type : Pharma / Healthcare/ Clinical research
Functional Area : Medical and Clinical
Req ID : 259871
End Date : 25th August, 2020
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