Parexel is hiring for the position of Clinical Database Programmer II in Bengaluru, Karnataka. This is a full-time opportunity within the clinical data management and database programming function, supporting clinical research and global biopharmaceutical studies.
The position is suitable for professionals with at least 3 years of experience in clinical data management or database programming. Candidates should have a bachelor’s degree in a relevant science discipline or equivalent work experience and knowledge of clinical database technologies, programming environments, regulatory requirements, and data standards.
The role involves building and maintaining clinical databases, developing consistency checks, supporting electronic case report form design, resolving technical requirements, and maintaining documentation required for quality and regulatory compliance.
Parexel Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Parexel |
| Job Title | Clinical Database Programmer II |
| Alternate Role | Clinical Database Build Programmer II |
| Department | Clinical Data Management / Database Programming |
| Location | Bengaluru, Karnataka |
| Job Type | Full Time |
| Experience | Minimum 3 Years |
| Qualification | Bachelor’s degree in relevant Science discipline or equivalent experience |
| Key Areas | Clinical Database Programming, EDC, CDMS, Data Management |
| Requisition ID | R0000045760 |
| Application Deadline | October 9, 2026 |
| Salary / CTC | Not specified |
About Parexel
Parexel is a global clinical development organization that provides clinical research and related services to the life sciences industry.
The company supports biopharmaceutical organizations and research sites in the planning and execution of clinical trials. Its work includes clinical development activities, data management, technology-enabled research processes, and other services supporting the development of new therapies.
Job Description
The Clinical Database Programmer II will support the development and maintenance of clinical databases used in clinical research.
The position involves technical work across clinical data management systems, including database development, programming, consistency checks, electronic case report form support, documentation, and quality-related activities.
The role requires an understanding of regulated clinical research environments and the ability to work with technical and cross-functional teams.
Clinical Database Programmer II – Role Overview
The position is focused on supporting clinical database activities from study planning and development through ongoing study operations and closeout.
The selected candidate will contribute to:
- Clinical database development.
- Database maintenance.
- Programming checks.
- EDC and CDMS activities.
- Technical documentation.
- Data quality processes.
- Regulatory traceability.
- Clinical data management standards.
Educational Qualification
Candidates should have:
- A Bachelor’s degree in a relevant Science discipline, or
- Equivalent relevant work experience.
The educational background should be relevant to clinical data management, programming, science, technology, or a related field.
Experience Requirements
Candidates should have at least:
3 years of experience in clinical data management or database programming.
Experience should ideally include work with clinical research databases, clinical data management systems, or programming environments used in clinical trials.
Programming and Technical Skills
Candidates should have experience with at least one relevant programming or database environment, such as:
- SAS
- CDMS
- EDC
- SQL
- VB
- Java
Experience with EDC systems, CDISC standards, and CDMS platforms is preferred.
Regulatory and Clinical Knowledge
Candidates should understand the requirements applicable to clinical research systems, including:
- ICH-GCP
- Applicable clinical research regulations
- 21 CFR Part 11
- Standard Operating Procedures (SOPs)
- System life-cycle methodologies
- Data quality requirements
- Regulatory documentation and traceability
Key Responsibilities
Clinical Database Development
The candidate will build and maintain clinical databases used for clinical research.
This may include databases supporting:
- Paper-based clinical systems.
- Electronic Data Capture (EDC) systems.
- Clinical data management activities.
Consistency Checks
The role includes developing and maintaining consistency checks to identify potential data issues.
These checks may follow:
- Standard formats.
- Project-specific requirements.
- CDISC-related formats where applicable.
Database Quality
The candidate will be expected to deliver high-quality database-related outputs and contribute to first-time quality of technical deliverables.
Attention to detail and proper verification are important aspects of the role.
Electronic Case Report Forms
The position includes providing technical input related to electronic Case Report Form (eCRF) design.
The candidate may work with project teams to identify technical requirements and support appropriate database implementation.
Technical Support
The programmer will assist with technical solutions for questions and requirements raised by internal teams and external clients.
This requires the ability to understand technical issues, analyze requirements, and communicate appropriate solutions.
Documentation and Compliance
The role involves maintaining supporting documentation required for:
- Regulatory compliance.
- System traceability.
- Project records.
- Technical standards.
- Database development activities.
The candidate will also document technical standards and any relevant deviations for project teams.
Standards and Process Development
The position may contribute to the creation and improvement of technical standards through:
- Tools.
- Programming libraries.
- Processes.
- Standardized approaches.
Required Skills
The ideal candidate should demonstrate:
- Clinical database programming knowledge.
- Clinical data management understanding.
- Experience with programming or database environments.
- Knowledge of EDC/CDMS systems.
- Understanding of clinical research processes.
- Strong attention to detail.
- Quality-focused approach.
- Good organizational skills.
- Ability to manage competing priorities.
- Problem-solving ability.
- Strong written and verbal English communication.
- Ability to learn new technical systems.
Work Location
Location: Bengaluru, Karnataka, India
Employment Type: Full Time
The supplied vacancy does not specify a remote or hybrid work arrangement.
Salary / CTC
The salary or CTC for the Clinical Database Programmer II position has not been disclosed in the supplied vacancy information.
Candidates can confirm compensation and other employment terms during the recruitment process.
Selection Process
The supplied job information does not provide a detailed selection process.
Candidates who meet the eligibility criteria may be contacted for further screening, technical discussions, interviews, or other recruitment stages.
How to Apply for Parexel Recruitment 2026
Eligible candidates can apply directly through the official Parexel careers portal.
Job Requisition ID: R0000045760
Application Deadline: October 9, 2026
Candidates should ensure that their resume clearly reflects their clinical data management/database programming experience and relevant technical skills.
Important Details Before Applying
- Position: Clinical Database Programmer II.
- Location: Bengaluru, Karnataka.
- Job type: Full Time.
- Minimum experience: 3 years in clinical data management or database programming.
- Qualification: Bachelor’s degree in a relevant science discipline or equivalent experience.
- Relevant technologies include SAS, CDMS, EDC, SQL, VB, and Java.
- EDC, CDISC, and CDMS experience is preferred.
- Knowledge of ICH-GCP and 21 CFR Part 11 is required.
- The role involves database development, consistency checks, eCRF support, technical documentation, and quality activities.
- Requisition ID: R0000045760.
- Application deadline: October 9, 2026.
- Salary/CTC is not specified.
Frequently Asked Questions
1. What is the job title at Parexel?
The position is Clinical Database Programmer II, also referred to as Clinical Database Build Programmer II.
2. Where is the job located?
The position is based in Bengaluru, Karnataka, India.
3. How much experience is required?
Candidates should have at least 3 years of experience in clinical data management or database programming.
4. What educational qualification is required?
A Bachelor’s degree in a relevant Science discipline or equivalent work experience is required.
5. Which programming technologies are mentioned?
The vacancy mentions SAS, CDMS, EDC, SQL, VB, and Java.
6. Is EDC experience mandatory?
Experience with EDC systems is listed as preferred rather than an absolute mandatory requirement in the supplied information.
7. Is CDISC knowledge required?
Knowledge of CDISC standards is preferred for the position.
8. Does the job involve clinical database development?
Yes. Database building and maintenance are central responsibilities of the role.
9. Does the role involve eCRF design?
Yes. The candidate will provide technical feedback related to electronic Case Report Form design.
10. Which regulatory requirements should candidates know?
The vacancy highlights ICH-GCP, applicable regulations, and 21 CFR Part 11, along with SOPs and system life-cycle methodologies.
11. What is the application deadline?
The stated application deadline is October 9, 2026.
12. What is the requisition ID?
The requisition ID is R0000045760.
13. Is salary mentioned?
No. The supplied vacancy does not disclose the salary or CTC.
Important Note
Recruitment requirements, eligibility criteria, application deadlines, vacancy status, and employment terms may change. Candidates should verify the latest information on the official Parexel careers portal before applying. Meeting the listed requirements does not guarantee selection or employment.