Pati Natabar
Clinical Research Associate @Aithent Inc
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WORK HISTORY
Clinical Research Associate @Aithent Inc
Chennai, IN
Ensure the integrity of data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations, and internal SOPs Prepare and maintain documents related to clinical trials.Generate data entry queries and test clinical applications for numerous clinical trials.Analyze clinical trials data and prepared reports for Data Coordinator and Sponsor.Serve as liaison between Data Management and other departments in Clinical application developments. Manage clinical research data for the new and ongoing clinical trials.Conduct UAT Testing and validate software application processes for the management of clinical trials.Assist with the creation of data manuals for specified clinical trials. Checked data for clinical trials and raised queries with any inaccuracies. Review and maintain data management documentation, record management systems and identify tracking tools. Ensure the accuracy and integrity of data entered in eCRF. Prepare reports and organize presentations or meetings about clinical trial progress.
EDUCATION
Berhampur University
Masters Degree, Biotechnology
ABOUT PATI NATABAR
Highly motivated M.Sc. Biotechnology graduate (Distinction) with a Diploma in Clinical Research, Clinical Data Management. Leveraging expertise in clinical research operations and data management to support the success of clinical trials in the biotechnology, pharmaceutical, and medical device industries.Key Skills and Experience:*Therapeutic area & Pipeline Analysis: Identified and assessed potential clients in the clinical research space, analyzing their therapeutic focus areas, pipelines, and clinical trial needs.*Clinical Research Operations: Conducted comprehensive reviews of FDA regulations and guidelines to ensure clinical trial protocols and data adhere to best practices.*Data Management: Performed meticulous data cleaning and validation activities to guarantee data accuracy and integrity for clinical research studies.Driven by a passion for clinical research and data management, I seek opportunities to utilize my academic background and professional skills to contribute to the advancement of science and medicine through robust clinical trial design and execution. I am eager to solve real-world problems and collaborate with innovative teams in the healthcare sector.
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