Required for Drug Safety Associate / Senior Drug Safety Associate in Icon Clinical Research - degree in pharmacy, science
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. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
Post: Drug Safety Associate / Senior Drug Safety Associate - 008559
This is an exciting opportunity to work within the Medical & Safety Services department at ICON, a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. As a Senior Drug Safety Associate in the validation team, you will be involved in the validation/QC of safety database fields on assigned projects and have the opportunity to progress into project management activities in the long term.
Overview of the Role
Your primary responsibility will be validating and quality checking safety database fields on assigned projects.
You will also provide input for and review relevant safety tracking systems for accuracy/quality and perform safety review of clinical data (case report forms) and patient labs.
You will also be responsible for documenting and processing serious adverse event cases within ICON, regulatory authorities and sponsor regulations and timeframes.
With a science degree, pharmacy or nursing background or equivalent, you will have previous experience in a drug safety environment together with strong knowledge of medical terminology.
You will have knowledge of drug safety databases, preferably ARGUS.
You will have the ability to produce high quality work, with meticulous attention to detail.
You will be fluent in verbal and written English, with excellent communication skills.
Location: Trivandrum, Chennai
Organization: Medical & Safety Srvs
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Pharmacovigilance, CR
End Date: 13th March, 2014
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