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Worldwide Clinical Trials

Senior Clinical Database Programmer

Worldwide Clinical Trials

. Coordinate and perform processes associated with configuration, maintenance, and validation of databases, database systems, and associated applications .

Posted 10/12/2026full-timeKochi • IndiaSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Data Management Systems and Software, with a strong focus on SAS Programming and CDISC SDTM standards. Capable of coordinating database configuration, maintenance, and validation while ensuring compliance with quality assurance and audit requirements.

Highest-signal resume keywords
SAS Programming LanguageData Management SystemsCDISC SDTM StandardsDatabase ConfigurationQuality Assurance

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Database MaintenanceData ValidationData ReconciliationData ListingsData TransfersEdit Check SpecificationsSAS Program DevelopmentDatabase TestingError ReportingSpecification Review
Soft Skills
Good Communication SkillsAttention to DetailProblem SolvingTeam Working SkillsCustomer Focus
Tools & Technologies
EDC SoftwareClinical Data Management SoftwareDatabase Upload Programs
Industry Keywords
Clinical Data ManagementQuality AssuranceAudit RequirementsData Entry SoftwareIT SOPs

About the role

Key responsibilities & impact
  • Coordinate and perform processes associated with configuration, maintenance, and validation of databases, database systems, and associated applications
  • Liaise with relevant staff to allocate tasks, establish timelines, report progress, and identify outstanding issues
  • Assist in training and mentoring Clinical Database Programmers in database configuration and SAS program development, testing, and execution
  • Assist in training and mentoring Data Management staff in database and SAS program specification
  • Review specifications for project-specific data entry software, including edit check specifications
  • Review validation plans for edit check and reconciliation check specifications
  • Develop, test, and run SAS programs for clinical data management, including data validation, reconciliation checks, data listings, and data transfers
  • Configure internal and third-party database/eDC software for Data Management, sponsors, and sites
  • Test databases and related applications according to IT and Data Management SOPs
  • Run database upload programs and process error reports
  • Liaise with third-party vendors to resolve software issues and implement changes
  • Liaise with sponsors or their designates regarding electronic data transfers
  • Support Data Management in producing and maintaining system procedures and documentation
  • Assist with Quality Assurance and audit requirements
  • Perform other duties as assigned

Requirements

What you’ll need
  • Educated to degree level or relevant experience
  • At least 5 years experience of Data Management Systems and Software
  • Understanding of CDISC SDTM standards
  • Experience of SAS programming language
  • Good written and verbal communication skills
  • Methodical and logical approach to problem solving
  • Ability to learn new tasks quickly
  • Close attention to detail
  • Ability to question the validity of data being entered/extracted
  • Hardworking and efficient
  • Good team working skills
  • Customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change
  • Computer literate and numerate
  • Willingness to adapt to various computer systems

Benefits

Comp & perks
  • Equal employment opportunity
  • Diverse and inclusive work environment
  • Supportive and collaborative teams
  • Training and mentoring opportunities
  • Professional development through exposure to innovative clinical data management work