Reeba Bose

I am Dr. Reeba Bose, a Pharm D graduate. After my graduation, Istarted working as an assistant clinical data coordinator and clinical Data coordinator at ICON Clinical Research, Trivandrum India in Apr 2019- Nov 2021. I have enough knowledge about the Microsoft tools like Excel, Word, and PowerPoint. Clinical Research subject from my Pharm D program provided me with immense knowledge about clinical research and the various healthcare professionals working on clinical Trials. My eagerness to work in clinical research led me to find a job in data management. I have enjoyed my profession and I am very pleased to continue my career in Clinical Research. Due to relocation and some family matters I have taken a 1-year career break and now I am very actively looking for a job in the clinical trial. My previous experience in protocol review, CRF guidelines, ICH-GCP guidelines, query writing, query resolution, listing review, all kind of vendor reconciliations, start-up, and close-out activities, UAT, and PPC activities will support my work as a good Clinical Trail Assistant. While working I have communicated with the Project manager, Clinical project manager, CRA, CTA, Medical Coders, Programmers, CDL, and sponsor to ensure a clean database. I have given training to site coordinators for a proper understanding of DM concepts mentored new team members and performed peer reviews.

Expertly reviewed case report form and data for completeness, compliance, accuracy, and consistency with all applicable procedures.  Communicated/coordinated with Project manager, Clinical project manager, CDL, and sponsor to ensure a clean database.  Performed listing reviews, external vendor system eCOA Reconciliation, Lab Reconciliations, IVRS Reconciliation, PK Reconciliation, PGx Reconciliation, and SAE Reconciliation.  Successfully trained site coordinators for proper understanding of DM concepts mentored new team members and performed peer review.  Evaluated and revised SOP’s-Data handling conventions, Manual review, and listing review to reflect current discrepancy management. Practices updated and authored CRF completionguidelines.  Initiated quality reviews, Identified all issues, and proposed resolutions.  Performed Data Access Training and User Access Training (UAT) to ensure the accuracy of thedatabase.  Participated in close-out activities and database finalization.

Accurately review the Case Report Form for completeness, accuracy, and consistency in accordance with all applicable procedures.  Performed Quality Reviews and appropriately identified all issues.  Performed DM review, Entry Freeze, and Hard lock.  Handling external vendor system _Lab Reconciliation.

Doctor of Pharmacy (Pharm D) Swamy Vivekananda College of Pharmacy Tamil Nadu Dr. M.G.R. Medical University Oct 2012- Dec 2018