Himani Hedaoo

About Himani Hedaoo

As a Clinical Data Coordinator at George Clinical, I have gained valuable experience in the field of clinical research. Working with databases such as RAVE, Merative Clinical Development (IBM), Clinion & Flatiron vessel (Protocol First), I have honed my skills in data cleaning and quality control checks to ensure accurate, complete, and consistent data collection. I have also conducted SAE & third-party data reconciliations and database lock activities to ensure that data is properly validated.In addition, I have performed User Acceptance Testing (UAT) for data entry screens, edits, and data review listings for all different roles used in the study. My experience in creating and updating the CRF/eCRF Completion Guidelines has helped me to better understand the importance of accurate and consistent data collection. I serve as a Subject Matter Expert (SME) for clinical laboratory data. Coordinated with teams including Biostatistics, Clinical Programming, Safety team, and Medical Coding.As an Intern in Clinical Data Management, I gained experience in data entry, review of discrepancy (edit check) output and validation listings based on data entered into the clinical database, and addressing queries in a timely manner as per the Data Management Plan (DMP) for the assigned projects. I also looked after the data entry process to ensure that data was entered accurately.With my strong communication, problem-solving, and team working skills, I am able to work effectively in a team environment to achieve study goals. My adaptability and willingness to learn make me a valuable asset to any team.My educational background in Certification of Clinical Research & Management, Master of Science in Biochemistry & Molecular Biology, and Bachelor of Science in Biotechnology, Biochemistry, and Chemistry, has equipped me with the necessary knowledge and skills to excel in the field of clinical research.My goal is to join a highly reputed and professional clinical research work environment where I can apply the best data management practices and experiences which will allow me to gain excellent advancement in my career. I have also completed the Clinical Trial Analysis and Reporting using SAS Programming certification from Internshala, which has further enhanced my skills in the field of clinical research.Overall, I am a highly motivated and results-driven Clinical Data Coordinator who is dedicated to ensuring that data for clinical trials are properly collected and validated. I look forward to contributing my skills and experience to a dynamic and innovative team.

Experience

1. Clinical Data Specialist

   IQVIA India

   Aug 2024 — Present · Bengaluru, IN

Education

• Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur

  Bachelor of Science - BS, Biotechnology

  2013 — 2016

• Pondicherry University

  Master's degree, Biochemistry and Molecular Biology

  2018 — 2020