Parexel is hiring for the position of Clinical Database Programmer II in Bengaluru, India. The role focuses on clinical database design, implementation, database programming, consistency checks, quality assurance, regulatory compliance, and support for clinical data management systems.
Job Details
| Job Details | Information |
|---|---|
| Company | Parexel |
| Position | Clinical Database Programmer II |
| Location | Bengaluru, India |
| Job Type | Full Time |
| Experience | At least 3 years |
| Qualification | Bachelor’s degree in a relevant science discipline or equivalent work experience |
| Job Requisition ID | R0000045760 |
| Application Deadline | October 9, 2026 |
Position: Clinical Database Programmer II
The Clinical Database Programmer II will support clinical research activities through database design, implementation, quality assurance, and technical solutions across clinical data management systems. The role involves collaboration with cross-functional and international teams and participation in study operations from planning through closeout.
Key Responsibilities
- Create, implement, and execute procedures for building and maintaining databases for paper-based and web-based EDC clinical data management systems.
- Build databases in standard or CDISC-compliant formats, including annotation of case report forms where applicable.
- Create, implement, and maintain consistency checks for database builds.
- Ensure database-related deliverables meet quality, accuracy, and compliance requirements.
- Provide technical feedback to study programmers developing electronic case report forms.
- Support technical solutions for internal and external client inquiries related to database design and implementation.
- Develop knowledge of clinical data management systems, EDC, clinical trial management systems, safety reporting, and programming languages.
- Maintain study documentation in accordance with standard operating procedures and guidelines.
- Maintain technical documentation for clinical databases and document deviations for project teams.
- Contribute to tools, libraries, and processes that support efficient database management practices.
Eligibility / Qualifications
Candidates should have:
- A Bachelor’s degree in a relevant science discipline or equivalent work experience.
- At least 3 years of experience in clinical data management or database programming.
- Experience in at least one programming environment such as SAS, CDMS, EDC, SQL, VB, or Java.
- Knowledge of standard operating procedures, guidelines, and system life cycle methodologies.
- Knowledge of ICH-GCP and applicable local and international regulations, including 21 CFR Part 11.
- Strong communication, organization, and problem-solving skills.
Required Skills
- Clinical database programming
- Clinical data management
- Database design and implementation
- EDC systems
- CDMS platforms
- Consistency checks
- CDISC standards
- SAS, SQL, VB, Java, or other relevant programming environments
- ICH-GCP
- 21 CFR Part 11
- System life cycle methodologies
- Technical documentation
- Quality and regulatory compliance
- Cross-functional collaboration
Preferred Qualifications
- Experience with electronic data capture (EDC) systems.
- Familiarity with CDISC standards and CDMS platforms.
- Experience in a clinical research or healthcare environment.
Candidate Profile
The role requires strong attention to detail and a commitment to quality in a regulated environment. Candidates should have excellent written and oral English communication skills, strong organizational abilities, problem-solving skills, and the ability to manage competing priorities.
The position also requires the ability to learn new systems, adapt to an evolving technical environment, collaborate with international teams, and work independently.
Application Details
