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.
r Planning and coordinating for the Protocol Training, Study Check-in activities with the study coordinator.
r Request, receive the Study Specific pre numbered forms & SOP forms in required number and maintain the timely accountability.
r 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.
r Preparation and compilation of TMF, Raw data, study schedule, Stations as required for the study.r r Call us on 76699-43030 & our team will get in touch with you.r r If the above job does not suit your profile, you can still apply as we have various vacancies across different cities & job areas.r r For details of other jobs, you can also email us, else check our websiter r Give a miss call on 76699-43030 & our team will get back to you within 3-4 business days.r r Thanksr r Hiring Team
r Canvas25 comr r Call : 76699-43030r r
Education: Any Graduate
Industry: Biotechnology/Pharmaceutical/Medicine, Healthcare
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