Summary
Overview
Work History
Education
Skills
Accomplishments
Core Skills
Availability
Timeline
Generic
Anjali Bhandarkar

Anjali Bhandarkar

Pune

Summary

Clinical Database Programmer with over 7 years of experience in Life Sciences and Clinical Trials, specializing in Medidata Rave and Oracle Inform for global studies. Demonstrated ability in end-to-end study build, validation, and database maintenance, consistently delivering high-quality results on time. Skilled in managing multiple studies simultaneously while ensuring data integrity and regulatory compliance. Currently enhancing expertise in SQL, Power BI, and Python for advanced clinical data analysis and reporting.

Overview

12
12
years of professional experience

Work History

Database Analyst/Programmer

IQVIA
Remote
02.2024 - Current
  • Worked as Clinical Database Programmer with excellent experience.
  • Programming of Derivations, Edit Checks.
  • Delivered studies with on time deliverables and with excellent quality 100% on-time delivery for Rave EDC.

Clinical Database Programmer

Accenture
Bangalore
09.2020 - 02.2024
  • Based on the specifications, designing standard and non-standard eCRFs, generating a logical edit check program to find the data inconsistency for EDC studies, validating the study and deployment.
  • Performing Unit Testing.
  • Resolve and update issues arising from QA/UAT including study databases, eCRFs and edit checks.
  • Involved in study design, Edit checks programming.
  • Archiving and Generating CSML.
  • Validating Study.
  • Creating Package and Deploying Study.
  • Accountable for high quality and on time delivery for assigned deliverables.

Associate Engineer

Pure Software Pvt Ltd
Hyderabad
08.2014 - 10.2018
  • Involved in study design, Edit checks programming.
  • Involved in unit testing and integration Testing.
  • Build test and maintain data bases.
  • Create and test data entry screens.
  • Program and generate project tracking reports.
  • Involved in writing test scripts, UAT of edit checks and taking reports from the server.
  • Understanding the requirement for each study and analyzing the possibilities.
  • Based on the specifications, designing standard and non-standard eCRF’s, generating a logical edit check program to find the data inconsistency for EDC studies.
  • Resolve and update issues arising from QA/UAT including study databases, eCRFs and edit checks.
  • Support any updates or changes to the study (e.g., protocol amendments); conduct change control process, and proper version control process, to production studies for both requested and approved changes.
  • Identify design issues, provide recommendations, and rise to the CDM in a timely fashion. Also provide feedback, suggestions for improvements to the design specifications or process.

Education

Bachelor of Engineering - Computer Science

Manoharbhai Institute of Engineering And Technology
Nagpur
09-2018

Skills

  • Clinical and EDC platforms
  • Database programming
  • Medidata Rave EDC
  • Oracle Inform
  • Central designer
  • Clinical Database Programming & CDM
  • Edit Check Programming
  • Dynamic Rules & Form Behaviors
  • Rave Architect
  • ECRF Design
  • UAT
  • Validation
  • Unit Testing
  • Troubleshooting
  • CSML
  • Deployment
  • Protocol Amendments
  • Impact Assessment
  • Issue Resolution\Investigation
  • Data Quality and compliance
  • Change control
  • eCRF design
  • Soft Skills
  • Strong communication & documentation skill
  • Managing Study deliverables
  • Experience in clinical study trial studies
  • Multi-study delivery management
  • Remote collaboration with global teams

Accomplishments

  • Achieved Start Business Award for the quarter of 2021 at Accenture.
  • Appreciated by the manager for work excellence in the Recognition Portal of Accenture.
  • Appreciated by the project lead for high-quality work and work excellence in the Spotlight Portal of Accenture.

Core Skills

Medidata Rave EDC, Oracle Inform, Central Designer, Edit Check Programming, Dynamic Rules and Form Behaviors, Rave Architect (Drafts, Forms, Fields), eCRF Design (configuration), UAT, Validation, Unit Testing, Troubleshooting, CSML, Deployment, Protocol Amendments, Impact Assessment, Troubleshooting, Issue Resolution, and good communication skills for effective collaboration with team members, managing study deliverables, and experience in clinical study trial studies with exposure to conduct activities

Availability

  • Open to full time remote or contract roles (USD-based with flexible overlap with US/ EU teams)

Timeline

Database Analyst/Programmer

IQVIA
02.2024 - Current

Clinical Database Programmer

Accenture
09.2020 - 02.2024

Associate Engineer

Pure Software Pvt Ltd
08.2014 - 10.2018

Bachelor of Engineering - Computer Science

Manoharbhai Institute of Engineering And Technology
Anjali Bhandarkar