ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies ICON enjoys a strong reputation for quality and is focused on staff development.
Post : Drug Safety Associate
Job Description
• As a DSA, you will be expected to perform case processing for serious adverse events, serious and non-serious adverse drug reactions and other medically-related project information such as adverse events of special interest and clinical endpoints.
• Provide input and review relevant safety tracking systems for accuracy and quality and assist with maintaining project files.
• Serve as a resource for investigational sites and ICON personnel on safety-related issues.
• Assist with generation of study specific procedures and with identifying out of scope activities in conjunction with the MSS Functional Lead.
Candidate Profile
• The successful candidate will have relevant clinical research / pharmaceutical industry experience, preferably in pharmacovigilance/drug safety, with knowledge of medical terminology and coding systems.
• Must be fluent in written and verbal English with good communication skills and basic computer skills. Detail orientated and capable of working effectively within a team environment.
• Medical / science background (nursing preferred) and/or bachelor’s degree or local equivalent.
Additional Information
Qualification : M.Pharm, B.Pharm
Location : Chennai
Industry Type : Pharma / Clinical research
Functional Area : Drug Safety
End Date : 10th March, 2023
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