Drug Safety Associate vacancy at Icon Clinical Research India Private Ltd

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Drug Safety Associate vacancy at Icon Clinical Research India Private Ltd

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 clinicalstudies .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.
 
Name of the Post : Drug Safety Associate
 
Name of the Institute : Icon Clinical Research India Private Limited
 
Desired Candidate Profile:The desired candidate will be responsible for monitoring and tracking Serious Adverse Events, serious and non serious drug adverse reactions and other medically related project information. You will ensure that all ICON, Sponsor and Regulatory timelines are met for the processing ad recording of safety information.
 
Job Description:You will be responsible for monitoring and tracking Serious Adverse Events, serious and non serious drug adverse reactions and other medically related project information. You will ensure that all ICON, Sponsor and Regulatory timelines are met for the processing ad recording of safety information.
 
Additional Responsibilities:
 
* Document and process serious adverse event reports within ICON, regulatory authorities and sponsor regulations and timeframes
* Provide input for and review relevant safety tracking systems fro accuracy and quality
* Perform safety review of clinical data (case report forms) and patient labs
* Assist medical monitor in documentation and processing routine exception and re-screen approvals
* Liaise with investigational sites and reporters on safety related issues
* Serve as medical resource to investigational sites and ICON personnel on safety related issues
* Perform safety related training for extra-department ICON staff
 
Experience and Qualification:
 
With a science degree , pharmacy or nursing background you will have a minimum of 8 months experience in a drug safety environment. You will possess excellent verbal and written communication skills and must be fluent in English. This will be combined with a good knowledge of medical terminology.
 
* In addition you will also require :
* Good basic computer skills in MS office applications and data base use
* Produce high quality work and be detail orientated
* Be able to prioritise your work to meet required deadline
* Be willing to travel up to 10%
 
You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.
 
Contact Details:
Company Name: Icon Clinical Research India Private Limited
Website:http://www.iconplc.com
Telephone:044-43902958
 
Candidates Interested to Apply for the Following Post Should send their CV’s to the following Email id : eval(unescape('%64%6f%63%75%6d%65%6e%74%2e%77%72%69%74%65%28%27%3c%61%20%68%72%65%66%3d%22%6d%61%69%6c%74%6f%3a%6d%61%6c%61%72%6b%61%6e%6e%61%6e%2e%6a%40%69%63%6f%6e%70%6c%63%2e%63%6f%6d%22%3e%6d%61%6c%61%72%6b%61%6e%6e%61%6e%2e%6a%40%69%63%6f%6e%70%6c%63%2e%63%6f%6d%3c%2f%61%3e%27%29%3b'))