Clinical Research Associate (BB-974BD)

Found in: Talent IN

Handling and execution of studies as per protocol, SOP and applicable regulatory requirements in a timely manner as per the agreed timelines in coordination with the study coordinator and Investigator.Planning and coordinating for the Protocol Training, Study Check-in activities with the study coordinator.Request, receive the Study Specific pre numbered forms & SOP forms in required number and maintain the timely accountability.Preparation of Master templates, Coordinating for the Check in activities on check-in day and ensuring the completion of Check-in. Ensure sufficient clinical supplies were in place for the study.Preparation and compilation of TMF, Raw data, study schedule, Stations as required for the study.If the above job does not suit your profile, you can still apply as we have various vacancies across different cities & job areas.For details of other jobs, you can also email us, else check our websiteGive a miss call on 76699-43030 & our team will get back to you within 3-4 business days.ThanksHiring TeamCanvas27 comCall 76699-43030

calendar_today21 hours ago


info full time

location_on Ahmedabad, India

work CANVAS27Odotcom

I expressly authorise the Terms and Conditions

Similar jobs