Oryxion is hiring a Clinical Database Programmer to support the design, development, and maintenance of clinical trial databases for global studies. This opportunity is ideal for candidates interested in Clinical Data Management (CDM), Electronic Data Capture (EDC) systems, and clinical trial data programming.
The role focuses on building eCRFs, configuring edit checks, validating clinical databases, and ensuring high-quality clinical trial data capture. Candidates who want to build a career in CRO clinical data programming, EDC database development, and CDISC-compliant clinical data systems will find this position highly valuable.
This job is particularly suitable for B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, or related graduates who want to work in clinical research organizations (CROs) and gain exposure to clinical database development and data quality management.
Job Overview
| Field | Details |
|---|---|
| Position | Clinical Database Programmer |
| Company | Oryxion |
| Experience | 0โ2 Years |
| Industry | Clinical Research / CRO |
| Department | Clinical Data Management |
| Employment Type | Full-Time |
Key Responsibilities
Clinical Database Development
- Design, build, and maintain clinical study databases in Electronic Data Capture (EDC) systems.
- Develop electronic Case Report Forms (eCRFs) based on study protocols and data management plans.
- Configure edit checks, field properties, and database logic to ensure accurate data capture.
- Ensure database builds comply with CDISC standards and clinical data management best practices.
Data Quality and Validation
- Perform User Acceptance Testing (UAT) and database validation activities.
- Develop and review edit checks and data validation rules.
- Identify and resolve data discrepancies and system issues during database testing and live studies.
Study Setup and Documentation
- Review clinical trial protocols, CRFs, and data specifications for accurate database setup.
- Maintain database build specifications, testing documentation, and change control records.
- Support database freeze and database lock activities before statistical analysis.
Project Delivery and Quality Compliance
- Ensure timely database builds, migrations, and updates aligned with study timelines.
- Follow SOPs, clinical data management standards, and regulatory guidelines.
- Support audits and regulatory inspections.
Cross-Functional Collaboration
- Work with Clinical Data Managers, Biostatisticians, Statistical Programmers, and clinical study teams.
- Assist with data review, database updates, and issue resolution.
- Participate in process improvements and automation initiatives within the clinical data management team.
Qualifications and Skills
Candidates applying for the Clinical Database Programmer job at Oryxion should have the following qualifications:
Education
- B.Pharm
- M.Pharm
- Pharm.D
- BSc / MSc Life Sciences
- Biotechnology or related fields
Experience
- 0โ2 years of experience in Clinical Data Management or Clinical Database Programming.
Technical Skills
- Experience with Electronic Data Capture (EDC) systems such as:
- Medidata Rave
- Oracle Clinical
- Veeva EDC
- Inform
- Knowledge of:
- CRF design
- Edit check programming
- Clinical trial data structures
- Clinical data validation
- Familiarity with CDISC standards is an advantage.
Core Competencies
- Strong analytical and problem-solving skills
- Excellent attention to detail
- Ability to maintain clinical trial data quality and compliance
- Effective communication and collaboration skills
Benefits of Working at Oryxion
- Exposure to global clinical trials and CRO operations
- Opportunity to work with advanced EDC systems and clinical databases
- Career growth in Clinical Data Management and Clinical Programming
- Collaborative and innovation-driven work environment
- Hands-on experience with clinical data standards and regulatory requirements
How to Apply
