Sr. Clinical Research Associate

Sr. Clinical Research Associate #lifesciencegraduate #nagpurjobs #apportunities #clinicalresearchinstitute #smo #clinicalresearchcareers #clinicalresearchtrials #medicalresearch #healthcare #biology #pharmacovigilance #clinicalresearchtraining #education #bpharma #research #clinicalresearchers #nurse #clinicalresearchjobs #crc #pharmaceuticals #pharma #clinicaltrialsguru #clinicaldatamanagement #cralife #sciences #pharmacy #training #careers #rn #clinicaltrialsday Essential duties: The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. Responsible for all aspects of study site monitoring including routine monitoring and close­out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned. Responsible for all aspects of site management as prescribed in the project plans. Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study. Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Monitor data for missing or implausible data. Ensure the resources of the Sponsor and Labcorp are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Labcorp travel policy. Ensure audit readiness at the site level. Travel, including air travel, may be required and is an essential function of the job. Prepare accurate and timely trip reports Manage small projects under direction of a Project Manager/Director as assigned. a. Serve as lead monitor for a protocol or project, and may assist in establishing monitoring plans and trip report review as assigned Review progress of projects and initiate appropriate actions to achieve target objectives. Organize and make presentations at Investigator Meetings. Participate in the development of protocols and Case Report Forms as assigned.