Job for Senior Drug Safety Associatein ICON Clinical Research
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: Senior Drug Safety Associate
* Complete all departmental project activities accurately in accordance with ICON SOPs, Study Specific Procedures, regulatory requirements, and Sponsors processes
* Review and process serious adverse events, spontaneously reported adverse reactions and/or other medically related information per assigned tasks and study specific procedures
* Provide input and review relevant safety tracking systems for accuracy and quality and assist with maintaining project files.
*Perform safety review of clinical and diagnostic data under supervision
A strong team player and a effective communicator with 2 years of relevant experience in drug safety / pharmacovigilance process will be the perfect fit for the role
Education: B.Pharm, B.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: drug safety / pharmacovigilance
End Date: 31st July, 2017
See All Other Jobs in our Database