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eCRF Designer I

REMOTE (IN)REMOTEPOSTED: 7/6/2026
PHARMAFull-time
HIRING ORGANIZATIONVEEDA LIFESCIENCESClinical Research Organization (CRO)
Veeda Lifesciences

ROLE DEFINITION & RESPONSIBILITIES

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 1–3 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.

Key Responsibilities

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

B.Pharm or M.Pharm degree.
1–3 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.

REQUIRED VERIFIED SKILLS

eCRF Designing
Clinical Data Management
Database setup
Edit checks
eTMF management
B.Pharm
M.Pharm

COMPENSATION & REWARDS

₹2.0L - 4.0L per annum
The expected salary of 2-4 LPA is highly competitive and standard for freshers and early-career data management professionals in the Indian clinical research industry.

ORGANIZATION CONTEXT & CULTURE

Veeda Clinical Research is a prominent Contract Research Organization (CRO) offering end-to-end clinical research services to pharmaceutical, biotechnology, and medical device companies worldwide. They specialize in early and late-phase clinical trials, bioequivalence studies, and comprehensive drug development support, including regulatory affairs, biostatistics, and medical writing.

TEAM SIZE: 1,001-5,000 employees
INDUSTRY: Clinical Research Organization (CRO)

EXPECTED CAREER ROADMAP

This role offers an excellent entry-point into Clinical Data Management, allowing professionals to progress into senior database designer, CDM lead, or clinical data manager roles within global CROs and pharmaceutical companies.

APPLICATION ADVISORY

To stand out, highlight any hands-on academic or professional experience with EDC platforms, database setup, or clinical trial protocols, and emphasize your knowledge of GCP guidelines.
RECOMMENDED TRAINING
1/5
The Clinical Data Management Blueprint

The Clinical Data Management Blueprint

READY TO SUBMIT?

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