X Ray Technician Mlt Medical Lab Technician Bsc Mlt Msc Mlt Medical Coding Analyst Medical Coding Freshers Medical Coder Trainee Medical Coder Clinical Pharmacy Physiotherapist Nutritionist Dietitian Food Technology Male Staff Nurse Female Staff Nurs
BDS, B.Pharma, B.Sc, B.Tech/B.E, BVSC, M.Pharma, M.Sc, M.Tech, MVSC
We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. Thats our vision. Were driven by it. And we need talented people who share it. If youre as driven as we are, join us. Youll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and youll be helping shape an industry. The role: 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. You will need: 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.