Veeda CR Hiring eCRF Designer I (Clinical Data Management)
Are you seeking Veeda Clinical Research Careers or a Clinical Data Management Remote Job? Leading Indian contract research organization (CRO) Veeda CR is hiring an eCRF Designer I for its Clinical Data Management department.
This clinical trials database design position is ideal for science or pharmacy graduates with 1 to 3 years of experience in Electronic Case Report Form (eCRF) building, database setup, edit checks preparation, and eTMF archiving. Freshers with relevant database course training are also welcome to apply. To draft a resume detailing your EDC database configuration or document indexing milestones, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Veeda Clinical Research (Veeda CR) |
| Position | eCRF Designer I |
| Employment Type | Full-Time |
| Work Location | Remote (Work From Home) |
| Hiring HQ Office | Ahmedabad, Gujarat, India |
| Experience Required | 1–3 Years (Freshers Can Apply) |
| Qualifications | B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc Life Sciences |
| Expected Salary | ₹2,00,000 – ₹4,00,000 per annum (CTC) |
💼 Key Responsibilities
- eCRF Designing: Design Electronic Case Report Forms (eCRFs) in compliance with clinical study protocols, EDC systems, and standard SOPs.
- Edit Checks: Prepare, implement, validate, and approve clinical database Edit Checks to ensure accurate data entry.
- Database Setup: Collaborate with CDM Study Leads during initial clinical database setup activities.
- eTMF Management: Create, organize, and archive clinical study documentation in accordance with eTMF plans.
- Protocol Amendments: Review protocol amendments and implement necessary changes in database structure and eCRFs.
- Quality Review: Conduct quality reviews of clinical databases to verify overall data integrity and GCP compliance.
To learn how entry-level eCRF designer salaries compare to specialized pharmacovigilance drug safety associate and clinical study coordinator structures, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master's degree in Pharmacy (B.Pharm, M.Pharm, Pharm.D) or life science postgraduate degrees (M.Sc, B.Sc Life Sciences).
- CDM Knowledge: Deep understanding of clinical data management guidelines, protocol reviews, and electronic data capture (EDC) systems.
- System Skills: Experience compiling database edit checks, handling metadata, and managing eTMF document libraries.
- Communication: Good written and verbal English communication, coordinating with data management and clinical operations teams.
For pharmacy graduates evaluating data management pathways compared to conventional laboratory quality control or formulation chemistry, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Veeda Clinical Research?
- Remote working model, offering flexible work-from-home options.
- Work with a leading Indian CRO partnering with global pharmaceutical companies.
- Hands-on learning across clinical database design and electronic validation tools.
- Collaborative and quality-oriented clinical research team.
To review your basic knowledge of clinical trial phases, safety report timelines, and GCP guidelines before your technical screenings, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 eCRF Designer vs Healthcare IT
eCRF Designers build electronic data collection forms, program edit check logic, and configure clinical databases, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Veeda CR Candidates
- Highlight EDC Platforms: Explicitly mention EDC databases (like Medidata RAVE, Oracle Clinical, or Veeva Vault) that you have worked on or trained in.
- Detail Edit Check Experience: State if you have experience writing logic specifications or validating automated queries for databases.
- List eTMF Knowledge: Mention if you have indexed, archived, or quality-checked investigator files in an eTMF system.
💬 Veeda CR eCRF Designer Interview Questions
- Q1. What is the basic purpose of an Edit Check in a clinical database?
Answer Guidance: Edit Checks are programmed logical validations that run inside an EDC system. They automatically flag discrepancies, outliers, or missing data during entry (e.g. alert if a patient's pulse is entered as 600 or if gender does not match pregnancy data). - Q2. How does a protocol amendment impact an active clinical database?
Answer Guidance: A protocol amendment may add new tests, change dosing schedules, or alter endpoints. The eCRF designer must review the changes, edit the database structure, add or modify eCRF pages, write new edit check validations, and test the update before taking the changes live. - Q3. Explain what an eTMF is and why it is critical for a clinical trial.
Answer Guidance: An eTMF (electronic Trial Master File) is a digital collection of essential study documents. It provides a complete audit trail of the study's design, conduct, and data quality, allowing inspectors to verify regulatory and GCP compliance.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Veeda CR's recruitment portal on Naukri. Click the button below to apply:
Apply Online – Veeda CR Naukri Portal❓ Frequently Asked Questions
Q. Is this eCRF Designer job remote?
Yes, this is a remote (Work From Home) opportunity based in India.
Q. Can freshers apply for the eCRF Designer I position?
Yes, fresh graduates with relevant clinical research qualifications or database certifications are eligible to apply.
Q. Which degrees are accepted by Veeda CR?
Veeda CR accepts B.Pharm, M.Pharm, Pharm.D, M.Sc, or B.Sc degrees in Life Science disciplines.
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