Summary
Overview
Work History
Education
Skills
Timeline
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PRANITH CHINTHREDDY

London,Ontario

Summary

Dedicated and detail-oriented Clinical Programmer with a strong background in developing and implementing clinical trial databases and programming solutions with 4+ Years of experience in the clinical domain with proficiency in tools like Oracle Clinical 5.0.1, iMedidata Rave, Data labs EDC, and Veeva Vault EDC. Basic knowledge of SQL and PL/SQL. Proven ability to collaborate with cross-functional teams, ensuring the efficient and accurate execution of clinical trial data management. Seeking a challenging position to contribute technical expertise and enhance the success of clinical research.

Overview

7
7
years of professional experience

Work History

Sr Clinical Programmer

Syneos Health
Toronto, ON
04.2022 - 12.2023
  • Led a team of database programmers at Syneos Health in the implementation and configuration of Medidata Rave for multiple clinical trials.
  • Oversaw the development and maintenance of custom Rave edit checks, validation procedures, and functions.
  • Collaborated with cross-functional teams to ensure the seamless integration of Medidata Rave into the overall clinical trial data management process.
  • Conducted training sessions for team members and provided ongoing support to ensure efficient use of Medidata Rave.
  • Managed project timelines, resources, and deliverables to ensure successful project completion.
  • Created and maintained data validation programs to ensure the quality and integrity of clinical trial data.
  • Worked closely with data managers and statisticians to address data-related issues and provide programming support.

Clinical Database Programmer

VIBGYOR INFORMATICS PVT LTD
Bangalore, India
09.2016 - 11.2019
  • Requirement gathering, Spec Review, Resourcing, Performing Impact analysis.
  • ECRF designing (Drafts, Folders, Forms, Fields) in iMedidata Rave, Data-Labs, and Veeva vault.
  • Edit check programming along with derivations.
  • Developing a clinical study from scratch to release into production.
  • Creating annotations and SAS or clinical views as required by the study team in rave.
  • Understanding of CRF's, eCRF's, protocol, and other documents of the study design.
  • Regular monitoring Review log from a shared location.
  • Responsible for tracking and deliverables of all the activities.
  • Working with other team members to resolve complex validation and derivation procedures.
  • Coordination with onsite team/client for clarifications/queries of requirements.
  • Peer review before study setup activities is delivered to the client.
  • Manage the overall quality of deliverables including the closure of all open QA issues
  • Ensuring training and audit compliance.
  • Planning and implementing continuous improvement for the process development.
  • · Performing activities related to post-production changes and migrations.

Education

Post-Graduation Diploma - Embedded Systems Development

Conestoga College Institute of Technology And Advanced Learning
Kitchener, ON
05.2021

Bachelor of Science - Electrical And Electronics Engineering

Jawaharlal Nehru Technological University (JNTUH)
India
04.2018

Skills

Tools:

Rave EDC, Data-labs EDC(PI), Oracle Clinical 501, Veeva vault, Base SAS

Languages:

SQL, PL/SQL, C, VB

Operating Systems:

Spreadsheet, MS Office 2007 (Word, Excel, PowerPoint)

MS-DOS, WINDOWS 95/98/NT

Timeline

Sr Clinical Programmer

Syneos Health
04.2022 - 12.2023

Clinical Database Programmer

VIBGYOR INFORMATICS PVT LTD
09.2016 - 11.2019

Post-Graduation Diploma - Embedded Systems Development

Conestoga College Institute of Technology And Advanced Learning

Bachelor of Science - Electrical And Electronics Engineering

Jawaharlal Nehru Technological University (JNTUH)

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PRANITH CHINTHREDDY