Ankit Boradkar
Database Management Analyst
Nagaur
Summary
In the Life Sciences domain, extensive experience in Clinical Data Management using Medidata Rave has been gained. As a certified Medidata Rave Study Builder, proficiency has been demonstrated in managing Clinical Trials, including study setup and conduct activities. These responsibilities encompass creating Case Report Forms (CRFs), implementing Edit Checks, Dynamics, Derivations, and handling Post-Production Changes. A detail-oriented team player with strong organizational skills, capable of handling multiple projects simultaneously with a high degree of accuracy. Furthermore, end-to-end Clinical Trial operations have been successfully managed in both Medidata Rave and Viedoc .
Overview
3
3
years of professional experience
6
6
years of post-secondary education
1
1
Certification
Work History
Database Management Analyst
IQVIA
Nagpur
08.2022 - Current
- Worked as Clinical Database Programmer with excellent experience in managing Clinical Trails as Lead Programmer for multiple sponsors.
- Programming of Derivations, Edit Checks and also experienced in working with Global Library. Excellent experience in Study Set up (Build) activities in creating eCRF's and suggesting possible solutions in implementing Post Production Changes.
- Post Production Changes with very good interpretation in Protocol Amendments. Coordinated with stakeholders to define project technical requirements.
- Delivered studies with on time deliverables and with excellent quality for both Classic Rave and Rave EDC.
- Ticketing and resolution for issues identified in studies at Production environment across multiple sponsors.
- Worked on Viedoc studies as Programmer and Database Designer.
Clinical Database Programmer
IQVIA
Mumbai
08.2022 - Current
- Programming of Derivations, Edit Checks and Coordinated with Study Lead Programmers on performing Migration Activities. Hands on experience in Study Set up (Build) activities in creating eCRFs.
- Recommend solutions to management for complex technical issues, providing feedback on DVS, PD Specifications, and CRF Completion Guidelines (CCG).
- Review and provide feedback on edit check documents, writing DVR logic according to study requirements, and conducting alpha testing.
- Create listings for RTDC and non-RTDC studies, including SAS-specific listings. Program edit checks in RAVE and Data-Labs EDC, documenting study functional test cases. Conduct peer reviews of programming and documentation, ensuring accuracy and compliance with study requirements.
Clinical Database Programming Intern
Parexel
Hydarabad
01.2022 - 06.2022
- Performed Review of Edit Check Specification and Classification of Edit checks and Custom Function. Validation Plan creation. Performed Data Entry for Validation Plan.
- Assisted Leads on Documentation and Report generation. Assisted in testing of newly developed applications for Project. Analyzed customer needs to create and implement appropriate solutions.
Education
Bachelor of Science - Pharmacy
Priyadarshini J.L.College of Pharmacy
Nagpur, India 08.2015 - 10.2021
Skills
- Clinical Study Database Design
- Edit Checks and Derivations
- Rave Migrations
- Viedoc
- Testing & Validation
- Problem-solving abilities
- Time management abilities
Certification
Medidata Rave Certified Study Builder
Timeline
Medidata Rave Certified Study Builder
08-2024
Database Management Analyst
IQVIA
08.2022 - Current
Clinical Database Programmer
IQVIA
08.2022 - Current
Clinical Database Programming Intern
Parexel
01.2022 - 06.2022
Bachelor of Science - Pharmacy
Priyadarshini J.L.College of Pharmacy
08.2015 - 10.2021
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