Looking for Clinical Programmer jobs in India? Atorus Research is currently hiring experienced professionals for the position of Clinical Programmer (EDC Programmer). This is a permanent remote opportunity ideal for candidates with experience in Medidata RAVE, Veeva EDC, clinical database programming, and clinical data management.
Candidates with a background in life sciences, pharmacy, biotechnology, or clinical research and experience in clinical database design and deployment are encouraged to apply.
Job Overview
| Job Details | Information |
|---|---|
| Position | Clinical Programmer (EDC Programmer) |
| Company | Atorus Research |
| Job Type | Full-Time, Permanent |
| Experience | 1–6 Years |
| Location | Remote (Hiring Office: Bengaluru, India) |
| Industry | Clinical Research / CRO |
| Department | Clinical Data Management |
| Openings | 2 |
About Atorus Research
Atorus Research delivers innovative clinical data solutions that help pharmaceutical, biotechnology, and healthcare organizations make faster and more informed decisions. Through advanced analytics, automation, and clinical technology platforms, Atorus simplifies complex clinical trial data processes while ensuring compliance with global regulatory standards.
Key Responsibilities
As a Clinical Programmer, you will be responsible for:
- Programming and configuring clinical databases using Medidata RAVE or Veeva EDC.
- Performing study setup activities according to approved specifications.
- Developing and maintaining edit checks and validation rules.
- Supporting database release and deployment activities.
- Reviewing Database Specifications and Data Validation Specifications (DVS).
- Ensuring compliance with SOPs, ICH-GCP guidelines, and sponsor requirements.
- Providing technical support for clinical data collection systems.
- Assisting Clinical Data Managers with reports, listings, and technical operations.
- Participating in study team meetings and departmental initiatives.
- Identifying project risks and communicating status updates to management.
Required Qualifications
Candidates should possess:
Educational Requirements
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Clinical Research, or related healthcare discipline.
- Equivalent certifications in allied health professions may also be considered.
Experience Requirements
- 1–6 years of experience in EDC programming.
- 1–4 years of experience in clinical database design and deployment.
- Experience working in Pharmaceutical, Biotechnology, or CRO environments preferred.
- Completion of training in Medidata RAVE, Veeva EDC, or similar EDC platforms.
Preferred Skills
- Medidata RAVE Programming
- Veeva EDC
- Clinical Database Management Systems (CDMS)
- Edit Check Programming
- Data Validation Specifications (DVS)
- Electronic Data Capture (EDC)
- Clinical Data Management
- Clinical Trial Database Design
- Good Clinical Practice (GCP)
- ICH Guidelines
- CRF Design and Validation
Benefits of Joining Atorus Research
- Permanent remote work opportunity.
- Exposure to global clinical development projects.
- Opportunity to work with leading EDC platforms including Medidata RAVE and Veeva.
- Career growth within clinical data management and clinical technology.
- Collaborative environment with experienced clinical research professionals.
- Competitive compensation and benefits package.
Why This Clinical Programmer Job is a Great Opportunity
The demand for Clinical Programmers, EDC Specialists, and Clinical Data Management professionals continues to grow across pharmaceutical and CRO industries. Professionals with expertise in Medidata RAVE, Veeva EDC, and clinical database programming are highly sought after as organizations accelerate digital clinical trial operations.
This role provides valuable exposure to global clinical studies while allowing the flexibility of a fully remote work environment.
How to Apply
