The clinical research industry continues to generate excellent career opportunities for pharmacy and life science professionals. If you have experience in Clinical Data Management (CDM) and are looking to advance your career in eCRF design, database setup, and clinical trial data management, Veeda Clinical Research (Veeda CR) has announced an exciting opening for the position of eCRF Designer I in Ahmedabad.

This opportunity is ideal for professionals with 1–3 years of Clinical Data Management experience who want to work on electronic Case Report Form (eCRF) design, edit check programming, database configuration, and clinical documentation while contributing to global clinical research projects.

Job Overview

Particular	Details
Company	Veeda Clinical Research (Veeda CR)
Position	eCRF Designer I
Location	Ahmedabad, Gujarat
Experience	1–3 Years
Qualification	B.Pharm / M.Pharm
Employment Type	Full-Time, Permanent
Industry	Clinical Research / CRO
Estimated Salary	₹2–4 LPA (As per job listing)
Vacancies	1

Educational Qualification

Candidates should possess one of the following qualifications:

B.Pharm
M.Pharm

Applicants with relevant Clinical Data Management experience and exposure to electronic data capture (EDC) systems will be preferred.

Key Responsibilities

As an eCRF Designer I, your responsibilities will include:

eCRF Design

Design electronic Case Report Forms (eCRFs) according to approved clinical study protocols.
Ensure eCRFs comply with company SOPs and regulatory requirements.
Support clinical studies through accurate electronic data collection design.

Edit Check Development

Develop logical edit checks and validation rules.
Improve clinical data quality through automated consistency checks.
Participate in edit check review and implementation.

Database Setup

Assist in configuring clinical study databases.
Support study startup activities.
Implement protocol amendments within study databases.

eTMF & Documentation

Prepare and maintain study documentation.
Organize Trial Master File (eTMF) documents.
Ensure documentation complies with quality standards.

Quality Review

Review study databases for completeness and consistency.
Participate in quality review activities.
Support change requests and protocol updates.

Required Skills

Candidates should possess knowledge of:

Clinical Data Management (CDM)
eCRF Design
Database Setup
Edit Check Development
Clinical Research Documentation
Protocol Interpretation
Standard Operating Procedures (SOPs)
Quality Review
Team Collaboration

Preferred Skills

Electronic Data Capture (EDC) Systems
Database Design
eTMF Management
Clinical Trial Documentation
Clinical Database Validation

Why Join Veeda CR?

This opportunity offers excellent exposure to modern Clinical Data Management processes.

Benefits include:

Work on global clinical trials
Exposure to electronic data capture systems
Hands-on experience in database development
Collaborative work environment
Permanent employment
Career growth in Clinical Data Management
Opportunity to work with experienced clinical research professionals

Who Should Apply?

This role is ideal for candidates who:

Have 1–3 years of Clinical Data Management experience.
Have knowledge of eCRF designing.
Understand clinical study protocols.
Possess database setup experience.
Are interested in clinical research documentation.
Want to build a long-term career in Clinical Data Management.

Job Location

Ahmedabad, Gujarat

Ahmedabad is one of India’s leading pharmaceutical and clinical research hubs, offering excellent career opportunities in CROs, pharmaceutical companies, biotechnology organizations, and healthcare research.

Career Growth After eCRF Designing

Professionals working in eCRF design can progress into roles such as:

Clinical Data Associate
Clinical Data Coordinator
Database Designer
Clinical Data Specialist
Clinical Data Manager
Lead Clinical Data Manager
Global Clinical Data Management Professional

With additional experience, professionals may also move into:

EDC Administration
Clinical Systems Management
Data Standards
Clinical Database Validation
Clinical Operations

Tips Before Applying

To improve your chances of selection:

Update your resume with your latest Clinical Data Management experience.
Highlight eCRF design and edit check development skills.
Mention any experience with EDC platforms.
Include clinical study documentation experience.
Review ICH-GCP guidelines and SOP compliance.
Demonstrate teamwork and communication skills.

Disclaimer

The information shared in this article is intended solely to inform job seekers about a publicly available employment opportunity. Job responsibilities, eligibility criteria, salary, and recruitment processes may change at the employer’s discretion. Candidates should verify all details through the employer’s official recruitment process before applying. This article is not affiliated with or endorsed by Veeda Clinical Research.

Apply Now

https://www.naukri.com/job-listings-ecrf-designer-i-veeda-cr-ahmedabad-1-to-3-years-060726006982?utmcampaign=androidjd&utmsource=share&src=sharedjd

Final Thoughts

For pharmacy graduates and Clinical Data Management professionals, this eCRF Designer I opportunity at Veeda Clinical Research offers an excellent platform to enhance expertise in electronic data capture, database design, edit check development, and clinical documentation. As clinical trials increasingly rely on advanced digital systems, skilled CDM professionals continue to be in high demand across the pharmaceutical and CRO industries.

If you have the required experience and are looking to grow your career in Clinical Data Management, this Ahmedabad-based opportunity could be your next significant career move.

Veeda CR Hiring eCRF Designer I (1–3 Years Experience) | Ahmedabad | Clinical Data Management Jobs 2026