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Diana Sebastian is a seasoned clinical professional with expertise in clinical data management, clinical research, and regulatory affairs. She has worked in various roles, including Clinical Trial Data Associate-II at PPD and Administrator SOP & Training at Bausch Health Companies Inc. Diana holds a Master's degree in Clinical Research from Cranfield University and a Bachelor of Science in Medical Microbiology from Kannur University.

Experience

  • The Applied AI Company (AAICO)
    • Abu Dhabi Emirate, United Arab Emirates
    • ML Analyst / Summarizer
      • Mar 2023 - Present
      • Abu Dhabi Emirate, United Arab Emirates

      -Code letters & other information received from care providers using the agreed practice protocols. Enter clinical data from letters & other information received from care providers, according to the practice protocol and as specified by the clinical team.-Detect, Interpret and update the treatment related information from the case of the patient which enable to convert physical health information into Electronic Medical Record (EMR).-Review and summarize medical information such as Attending Physician Statements, lab reports, paramed exams, and/or other related underwriting information consistent per client specifications-Be aware of specific Read Codes and associated records; following Practice protocols for recording,obtaining and filing patient records as appropriate -Adhere to and monitor progress of notes summarising against Practice targets, maintainingstructure and protocols when recording new information.-Interaction with managers regarding problem solving and understanding the process.

  • Bausch Health Companies Inc.
    • United Arab Emirates
    • Administrator Sop & Training
      • May 2020 - Jan 2021
      • United Arab Emirates

    • United States
    • Research Services
    • 700 & Above Employee
    • Clinical Trial Data Associate- II
      • May 2017 - May 2019

      Identifies, resolves, and updates data discrepancies. Makes changes to the datamanagement database as required. Generates, tracks and resolves data clarifications and queries. May implement CRF design in identified graphic design package. Produces project-specific status reports for CDM management, PM and/or clients on a regular basis. Creating study metrics.To be actively involved in implement the process improvement and learnings of previous studiesDatabase testing of assigned studies.Reviews data listings for accuracy and consistency of data. Analyzes and resolves data validation and other data management reports. Produces project-specific status reports for CDM management and for clients on a regular basis. Performs data management activities such as Serious Adverse Event and Third Party Vendor reconciliations as well as Data Listing reviews.

    • Clinical Trial Data Associate-I
      • May 2016 - Apr 2017

      Identifies, resolves, and updates data discrepancies. Makes changes to the datamanagement database as required. Validation procedures testing for assigned studies.Data Reconciliations/Lab reconciliationCreating MetricsGenerates, tracks and resolves data clarifications and queries.May implement CRF design in identified graphic design package.

    • clinical data management
      • Apr 2014 - Jul 2014
      • banglore

      1. data entry into database2. delivery of assigned work according to assigned timelines3.compliance with the project specific procedures.4.coordination with the project team5.reporting to the project lead

Education

  • 2014 - 2016
    Cranfield University
    Master's degree, CLINICAL RESEARCH
  • 2010 - 2014
    Kannur University
    Bachelor of Science (BSc), Medical Microbiology

Suggested Services

This profile is unclaimed. These are suggested service rates with 0% commision upon successful connection

Industry Focus. “Technology, Information and Internet”

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