Looking for Clinical Data Management jobs in India? Veeda CR is hiring an eCRF Designer I for its Clinical Research team. This is an excellent remote pharmaceutical job for candidates with 1โ3 years of experience in eCRF designing, Clinical Data Management, database setup, edit checks, and eTMF management.
If you have a B.Pharm or M.Pharm degree and experience in clinical research databases, this opportunity allows you to work remotely while contributing to clinical trial data quality and regulatory compliance.
Job Details
| Particular | Details |
|---|---|
| Company | Veeda CR |
| Position | eCRF Designer I |
| Job Type | Full-Time |
| Experience | 1โ3 Years |
| Qualification | B.Pharm, M.Pharm |
| Location | Remote (Hiring Office: Ahmedabad) |
| Salary | โน2โ4 LPA (Expected) |
| Industry | Pharmaceutical & Clinical Research |
Key Responsibilities
As an eCRF Designer I, your responsibilities will include:
- Design Electronic Case Report Forms (eCRFs) according to study protocols and SOPs.
- Prepare, implement, validate, and approve Edit Checks.
- Create, organize, and maintain study documentation as per eTMF Plans.
- Collaborate with Study Leads during clinical database setup.
- Perform quality review of clinical study databases.
- Review and recommend modifications to CRFs and databases after protocol amendments.
- Ensure compliance with GCP, SOPs, and clinical research standards.
- Support Clinical Data Management activities across multiple studies.
Eligibility Criteria
Candidates should possess:
- B.Pharm or M.Pharm degree.
- 1โ3 years of experience in Clinical Data Management.
- Hands-on experience in eCRF Designing.
- Knowledge of eTMF documentation.
- Experience with Edit Check preparation and validation.
- Understanding of Clinical Trial Protocols and SOPs.
- Familiarity with database setup activities.
- Strong documentation and communication skills.
Preferred Skills
- Clinical Data Management
- eCRF Design
- Electronic Data Capture (EDC)
- eTMF Management
- Database Design
- Protocol Review
- Edit Checks
- Quality Review
- Clinical Research Documentation
- SOP Compliance
- Good Clinical Practice (GCP)
Why Join Veeda CR?
Working at Veeda CR offers professionals an opportunity to:
- Work remotely with flexible collaboration.
- Build expertise in Clinical Data Management.
- Gain experience in global clinical research projects.
- Work with experienced Clinical Research professionals.
- Enhance skills in eCRF development and database management.
- Grow your career in the pharmaceutical and CRO industry.
How to Apply
