Parexel Careers 2026 | Principal Clinical Database Programmer Jobs

📋 Job Overview

• Company: Parexel
• Position: Principal Clinical Database Programmer
• Job Requisition ID: R0000043624
• Job Locations: Hyderabad, Telangana | Bengaluru, Karnataka
• Employment Type: Full-Time
• Experience: 8+ Years in Clinical Data Programming
• Qualification: Bachelor’s degree in a relevant science discipline (preferred) or equivalent experience
• Core Technology focus: Medidata Rave, InForm, Veeva, SAS, SQL

💼 Key Responsibilities

• EDC Systems Build: Lead and execute database setups, eCRF configurations, and database revisions for clinical trial management systems.
• Edit Check Programming: Write and validate consistency checks and edit checks in CDISC-compliant formats.
• Project Management: Coordinate programming study teams, negotiate database timelines, and monitor resourcing budgets.
• Sponsor Communications: Serve as the primary technical point of contact for external pharmaceutical clients and internal data management leads.
• Database Lock Tasks: Perform lock/unlock steps on clinical databases in accordance with regulatory guidelines and standard SOPs.
• Integrations: Support the integration of third-party clinical databases (CTMS, Coding systems, Safety databases) with EDC networks.
• SME & Mentorship: Act as a Subject Matter Expert (SME) on systems like Medidata Rave, providing technical solutions and mentoring junior programmers.

To learn about how clinical programming compares with database management and analytical programming, review our overview on Clinical SAS vs Clinical Data Management.

🎓 Required Qualifications & Skills

• Education: Bachelor’s degree in a science or technology field (or equivalent clinical experience).
• Programming Experience: Minimum 8 years in clinical database programming.
• Language Skills: Proficiency in at least one environment (SAS, SQL, VB, Java, CDMS).
• EDC Platforms: Hands-on experience with at least two systems (e.g., Medidata Rave, InForm, DataLabs, Veeva Safety/EDC). Rave/InForm certified builds are preferred.
• Regulatory Knowledge: Strong understanding of ICH-GCP, SDLC methodologies, and FDA 21 CFR Part 11 electronic record rules.
• Leadership: Proven experience coordinating clinical project teams and leading virtual teams across multiple time zones.

To learn about standard interview questions, clinical data review steps, and quality standards in CDM, see our guide on Clinical Data Management (CDM) Interview Questions.

🎁 Why Join Parexel?

• Work for a premier global CDMO and CRO collaborating on advanced global clinical drug studies.
• Lead complex, multi-site eClinical data projects using state-of-the-art database tools.
• Access global technology training platforms, professional development, and corporate benefits.
• Stable, high-impact career path with direct pathways to move into technology management.

📝 Resume Tips for Principal Programmer Candidates

• List Database Certifications: Clearly state if you are a Certified Medidata Rave Study Builder or hold Inform certificates.
• Detail Project Scale: Mention the number of active database builds you supervised and the budget scopes managed.
• Specify Standards Knowledge: Highlight your experience with CDISC standards (SDTM, CDASH) and Computer System Validation (CSV) protocols.

💬 Parexel Principal Programmer Interview Questions

• Q1. What are the key stages of the Software Development Life Cycle (SDLC) in database setup?
  Answer Guidance: In clinical programming, SDLC stages include Requirement Analysis (reviewing CRF designs), Database Design (eCRF layout configuration), Programming (writing edit check scripts), Testing/UAT (User Acceptance Testing by data managers), Deployment (pushing database to production), and Maintenance/Decommissioning (database lock and closeout).
• Q2. How do you implement CDISC standards during eCRF design?
  Answer Guidance: I align database fields with CDASH (Clinical Data Acquisition Standards Harmonization) standards. This ensures that variables are named and structured consistently from data collection (EDC) through to analysis datasets (SDTM), optimizing regulatory submission pipelines.
• Q3. Explain how you manage a change control request after a database has gone live.
  Answer Guidance: I evaluate the impact of the request on existing data and study timelines. Once approved, I draft the technical specifications, implement the changes in the development environment, execute user testing to ensure no data is lost or corrupted, obtain approvals, and schedule the migration to the live environment according to SOP guidelines.

📖 How to Apply?

Before submitting your application, please read our step-by-step guidance on how to navigate Workday registration portals, fill out profiles, and format your application:

👉 Read Step-by-Step Application Guide

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Want to build a professional ATS-friendly resume tailored for Clinical Database Programming, eClinical systems design, or CDISC database builds? Message us directly on our LinkedIn Company Page with the phrase “I want Resume Builder Service”, and our expert team will connect with you:

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❓ Frequently Asked Questions

Q. What is the minimum experience required for this Principal role?
Candidates must have at least 8 years of clinical data programming or clinical systems setup experience.

Q. Where are these positions based?
The positions are based full-time out of Parexel’s sites in Hyderabad and Bengaluru.

Q. Which databases should the candidate be familiar with?
Candidates should have strong experience working with at least two systems used in clinical trials, such as Medidata Rave, InForm, DataLabs, Veeva Safety, or SAS.