Are you an experienced Clinical Data Management (CDM) professional looking for a remote opportunity in the clinical research industry? If you have expertise in electronic Case Report Form (eCRF) design, database development, and clinical trial data management, this could be the right opportunity for you.

A leading life sciences organization is currently inviting applications for the position of eCRF Designer / Clinical Data Management (CDM) Associate. This role offers the flexibility of working remotely while requiring occasional travel to the Ahmedabad office whenever project requirements demand.

If you’re passionate about ensuring high-quality clinical trial data and contributing to global research projects, read on to learn more.

Job Details

Job Role	eCRF Designer / Clinical Data Management (CDM) Associate
Experience	2–4 Years
Qualification	Bachelor’s or Master’s Degree in Pharmacy, Life Sciences, Biotechnology, or related field
Job Location	Ahmedabad, Gujarat
Work Mode	Remote (Travel to Ahmedabad office when required)
Industry	Clinical Research / Life Sciences

About the Opportunity

Clinical Data Management plays a critical role in ensuring that clinical trial data is accurate, complete, and compliant with regulatory requirements. Every successful clinical trial depends on well-designed electronic databases and efficient data management processes.

As an eCRF Designer / CDM Associate, you will work closely with clinical operations teams, study leads, and project managers to develop electronic case report forms, implement edit checks, maintain database quality, and support clinical studies from startup through completion.

This position is ideal for professionals who enjoy working with Electronic Data Capture (EDC) systems and contributing to high-quality clinical research.

Key Responsibilities

The selected candidate will be expected to perform responsibilities such as:

Design electronic Case Report Forms (eCRFs) according to approved study protocols.
Develop, test, validate, and implement edit checks to ensure high-quality clinical data.
Coordinate database development activities with Study Leads and project teams.
Maintain Trial Master File (eTMF) documentation related to database development.
Participate in study reviews and database quality assessments.
Support protocol amendments and required database modifications.
Ensure compliance with SOPs, GCP guidelines, and organizational standards.
Collaborate with cross-functional clinical research teams.
Review database consistency before study deployment.
Assist in troubleshooting database-related issues during ongoing studies.

Educational Qualification

Applicants should possess one of the following qualifications:

B.Pharm
M.Pharm
B.Sc Life Sciences
M.Sc Life Sciences
Biotechnology
Microbiology
Biomedical Sciences
Any relevant healthcare or life sciences discipline

Experience Required

Candidates should have:

2–4 years of Clinical Data Management experience
Hands-on experience in eCRF design
Knowledge of Electronic Data Capture (EDC) systems
Experience with edit check programming
Understanding of clinical trial documentation
Familiarity with database validation processes
Experience in HVS BABE trials (Preferred)

Desired Skills

Successful candidates are expected to possess:

Strong analytical skills
Excellent attention to detail
Knowledge of Good Clinical Practice (GCP)
Understanding of clinical trial workflows
Database management expertise
Documentation skills
Problem-solving ability
Time management
Communication skills
Team collaboration
Quality-focused mindset
Adaptability in remote work environments

Why You Should Apply

This opportunity offers several attractive benefits for experienced Clinical Data Management professionals.

Remote Working Flexibility

Enjoy the convenience of working remotely while contributing to important clinical research projects.

Career Growth

Gain valuable exposure to clinical database development and electronic data capture systems used in global clinical trials.

Collaborative Environment

Work alongside experienced Clinical Data Management professionals, Study Leads, and Clinical Operations teams.

High Industry Demand

Clinical Data Management remains one of the fastest-growing functions within pharmaceutical companies, CROs, and biotechnology organizations.

Who Should Apply?

This opportunity is suitable for professionals who:

Have experience in Clinical Data Management.
Want to work remotely.
Have expertise in eCRF design.
Are interested in database development.
Enjoy maintaining data quality.
Have worked on clinical trial databases.
Wish to advance their career in clinical research.

Tips to Increase Your Chances of Selection

Before submitting your application, make sure your resume highlights:

Clinical Data Management experience
eCRF design projects
EDC platforms you’ve worked on
Database build activities
Edit check programming
Clinical trial experience
Protocol amendment support
GCP knowledge
eTMF documentation
Team collaboration achievements

Recruiters often shortlist candidates whose resumes clearly demonstrate relevant project experience and measurable contributions.

How to Apply

Interested and eligible candidates can apply by sending their updated resume to the recruitment team.

Email: Sunil.K2761@veedalifesciences.com

Subject Line Suggestion: Application for eCRF Designer / CDM Associate

It is recommended to apply as early as possible, as applications may close once suitable candidates are identified.

Career Scope in Clinical Data Management

Clinical Data Management continues to be one of the most promising career paths in the pharmaceutical and clinical research industry. Professionals with expertise in eCRF design, EDC systems, and database management are increasingly sought after by Contract Research Organizations (CROs), pharmaceutical companies, biotechnology firms, and medical device organizations.

With experience, professionals can progress into roles such as:

Senior Clinical Data Manager
Clinical Database Programmer
Lead CDM Associate
Data Management Lead
Clinical Systems Specialist
Clinical Project Manager

As the demand for decentralized and digital clinical trials grows, skilled CDM professionals can expect strong career prospects and continuous learning opportunities.

Final Thoughts

If you have 2–4 years of experience in Clinical Data Management and are looking for a flexible remote opportunity, this role offers an excellent platform to further your career. From designing eCRFs to supporting high-quality clinical trial databases, you’ll have the opportunity to contribute to meaningful research while expanding your professional expertise.

Ensure your resume is updated, emphasize your relevant technical skills, and submit your application promptly to maximize your chances of being shortlisted.

We wish you all the best in your clinical research career!

Frequently Asked Questions (FAQs)

Is this a remote job?

Yes. The position is primarily remote, with occasional travel to the Ahmedabad office based on project requirements.

What experience is required?

Candidates should have 2–4 years of experience in Clinical Data Management, including hands-on experience in eCRF design.

Which educational qualifications are accepted?

Bachelor’s or Master’s degrees in Pharmacy, Life Sciences, Biotechnology, or related healthcare disciplines are preferred.

Is experience in HVS BABE trials mandatory?

No. It is preferred but not mandatory.

How can I apply?

Eligible candidates can send their updated resume to Sunil.K2761@veedalifesciences.com.

Focus Keyword

eCRF Designer Jobs

eCRF Designer / Clinical Data Management (CDM) Associate Hiring – Remote Opportunity in Ahmedabad | Apply Now