Regulatory Associate - Level 1 US
Preparation of high quality, regulatory labeling documents (prescribing information, patient leaflets) using varied information sources. Liaising closely with other GSK personnel to ensure accuracy of draft prescriber information or patient information. Working to agreed deadlines and maintaining records reflecting project status. Responsible for highlighting potential delaying factors promptly to line management and sharing knowledge of regulatory documentation and procedures with others to assist in problem solving.
Health care professional (e.g., PharmD) preferred. Prior experience in strategic labeling development or drug information preferred.
Excellent communication skills, strong attention to detail, strong writing skills, and ability to synthesize and summarize clinical and pharmaceutical data are a must.
SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
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