Chennai; Drug Safety Associate -- All Levels; B.Pharm, M.Pharma; Icon Clinical Research India Private Limited

Experience: 6 months - 3 Years

Location: Chennai

Desired Candidate Profile

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.



Job Description
• 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.

Come to ICON and be an important part of a well respected and growing company that believes the details of your career are every bit as critical as the work you do. You'll enjoy highly competitive compensation and an exceptional benefits package

send resumes to:
Nilamadhab.Mahapatra@iconplc.com