Clinical Trial SME @ Icon .."R"

Clinical Trial SME
Icon Clinical Research India Private Limited - India

Review clinical trial protocols and identify possible vulnerabilities and present your findings to the production team using you clinical knowledge and experience to provide direction for the project Attend meetings with the clients as needed and attend daily team scrums and provide clinical input as needed on all study components. Provide the clinical guidance and expertise necessary to assist in the production of our product offering in particular drawing on experience from on-site monitoring and daily interaction with clinical sites. Technically review all production scripts to ensure technical accuracy and relevance to the end user (i.e. Investigators and Site Staff). Work closely with the project PM to ensure the delivery of an on-time and high quality product beneficial to those who work on the trial and ensuring maximum usage by the end user. Ensure the maintenance of a high personal level of knowledge concerning current regulation and changes within the clinical research industry by means of internal support and individual learning. Role Requirements B.Sc. (Hons) in life science or equivalent. At least 2 years experience as a Clinical Research Associate/site monitor or equivalent within the clinical research industry. CLICK HERE TOVIEW / APPLY