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Ensure Visit Reports are written and submitted via CTMS within 5 working days of visit.Ensures proper storage, dispensation, and accountability of all Investigational Product(s) and trial-related materials.Developed recruitment strategies and an enrollment plan with the investigator and site staff to meet recruitment goals in coordination with the SOP and GCP guidelines.Coordinated with investigators and site workers to ensure that the protocol is being adhered to while checking for Protocol deviations throughout the course of the study.Conducted site management activities, including but not limited to site selection visits, site initiation visits, site training, site routine monitoring visits, and site close out visits.Assisted the data management groups and the project team in the processing of all clinical data by ensuring the timely collection of other aspects of job-related responsibilities data and query resolution.Looking for drafting your winning cover letter? See our sample Clinical Research Associate Cover Letter. To become a CRA, candidates should have a degree or PG degree in life science, medical science, or nursing. As this job involves documentation and recording tasks, candidates are supposed to have thorough computerized processing skills and understand the importance of clinical practices too. Apart from coordinating the process results the clinical research associates are involved in disbursing such duties as – developing trial products, presenting trial protocols, designing data collection forms, liaising with investigators, monitoring the trail throughout the project, verifying data, setting up trial sets, writing visit reports, closing down trial sites and wiring technical trial reports for submission.Ī well-drafted Clinical Research Associate Resume emphasizes on skills and qualifications such as – excellent communication skills, relationship building abilities, numeracy skills, and eye to details, multitasking skills, the ability to collect data and good IT skills. Clinical Research Associate Resume SamplesĬlinical research associates are involved in collecting and organizing data that are obtained from trials and studies made from pharmaceuticals and biotechnology.