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Parexel

Clinical Database Programmer II

Parexel

Clinical Database Programmer II at Parexel overseeing programming activities in clinical trials. Responsible for database setup and regulatory compliance with required documentation.

Posted 7/16/2026full-timeHyderabad • 🇮🇳 IndiaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Clinical Data Programming and adherence to regulatory standards, including ICH-GCP and 21 CFR Part 11. Proficient in setting up databases and maintaining documentation for clinical trials.

Highest-signal resume keywords
Clinical Data ProgrammingSASCDMSEDCSQL

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Data ProgrammingDatabase SetupSASCDMSEDCSQLVBJavaSOPsICH-GCP
Industry Keywords
Clinical TrialsService Level AgreementsDocumentationStandards Creation21 CFR Part 11

Tech Stack

Tools & technologies
Google Cloud PlatformJavaSQL

About the role

Key responsibilities & impact
  • Provide technical expertise for the conduct of clinical trials
  • Support various programming activities related to clinical systems
  • Setup databases for clinical data management systems
  • Ensure adherence to service level agreements
  • Maintain supporting documentation for studies
  • Participate in the creation of standards as required for GDO

Requirements

What you’ll need
  • 3 to 5 years of experience in Clinical Data Programming
  • Experience in at least one programming environment (e.g. SAS, CDMS, EDC, SQL, VB, Java)
  • Knowledge of SOPs/Guidelines/Work Instructions/System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.
  • Bachelor's degree (or equivalent) in a relevant science discipline is preferred or equivalent work experience.

Benefits

Comp & perks
  • Health insurance
  • Flexible working hours
  • Professional development