GlaxoSmith Hirirng Senior Scientific Writer M.Pharm /
Freshers with Ph.D degree can also be considered Apply Now
Job
Description
Basic qualifications:
6+ years of experience in
Regulatory Writing and ICH Guideline.
M.Pharm / Freshers with Ph.D degree can also be considered.
M.Pharm / Freshers with Ph.D degree can also be considered.
Responsibilities:
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.
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