Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Ecrf / Database Developer Bengaluru, Karnataka, India

Smartrecruiters
smartrecruiters
3-6 years
Not Disclosed
Bengaluru, Karnataka, India
10 Feb. 17, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: eCRF / Database Developer
Location: Bengaluru, Karnataka, India
Job Type: Full-time
Experience Required: 3–6 years (relevant experience in EDC/eCRF development and clinical data management)

Company Overview
Eurofins Scientific is a global leader in life sciences, delivering a comprehensive portfolio of analytical testing services across multiple industries. The organization is recognized for its leadership in food, environmental, pharmaceutical, and cosmetic product testing, as well as agroscience CRO services. Eurofins also holds a strong global presence in genomics, discovery pharmacology, forensics, CDMO services, advanced material sciences, and clinical study support.

With a global network of laboratories across multiple countries and a workforce of thousands of professionals, Eurofins provides innovative testing solutions and specialty diagnostic services worldwide. Eurofins Technologies, a specialized business division, focuses on the development and commercialization of bioanalytical technologies and diagnostic test kits, supporting food safety, environmental safety, animal health, and clinical diagnostics sectors.

Eurofins Central Laboratory, a dedicated global organization within the group, supports all phases of clinical trials through advanced central laboratory services and GLP-compliant capabilities.

Job Overview
The eCRF / Database Developer will be responsible for designing, developing, validating, and managing electronic case report forms (eCRFs) and clinical databases in alignment with clinical study protocols. The role involves supporting clinical data management processes, ensuring high-quality data capture, and maintaining compliance with regulatory and organizational standards.

Key Responsibilities

  • Assess database design requirements related to data capture tools, data extraction, processing, and reporting.

  • Design and develop clinical databases based on study protocols and clinical data manager specifications.

  • Provide technical recommendations and solutions for complex database and data management challenges.

  • Configure and validate dataset mapping for data exports from Electronic Data Capture (EDC) systems.

  • Program and implement edit checks according to defined clinical data specifications.

  • Support issue resolution and required updates to eCRFs and edit checks during system testing, User Acceptance Testing (UAT), and deployment phases.

  • Import and manage external data within EDC platforms in accordance with data transfer agreements.

  • Manage multiple clinical studies simultaneously while ensuring timely project delivery.

  • Support or manage edit check testing and UAT processes when required.

  • Archive study databases and maintain associated documentation.

  • Participate in the review and development of quality documentation, including Standard Operating Procedures (SOPs) and best practices.

Qualifications and Skills

  • Bachelor of Science degree or equivalent qualification in a relevant field.

  • Proven experience in EDC and eCRF design and development based on clinical study protocols.

  • Strong understanding of clinical research processes and clinical data management workflows.

  • Hands-on experience creating eCRFs using EDC tools such as Oracle RDC, Lifesphere, Ennov, Inform, or similar platforms.

  • Experience collaborating with cross-functional clinical study teams to meet project timelines and deliverables.

  • Knowledge of data management tools, technologies, and regulatory requirements.

  • Ability to learn new processes, systems, and programming languages efficiently.

  • Strong analytical thinking and problem-solving capabilities.

Professional Attributes

  • Structured and detail-oriented approach to work.

  • Strong communication and collaboration skills.

  • Ability to manage multiple priorities in a fast-paced environment.

  • High level of professionalism aligned with global quality standards.

  • Adaptability and willingness to take on increasing responsibilities in a growing organization.

Career Growth Opportunities
As part of a rapidly expanding global organization, high-performing professionals may receive opportunities for expanded responsibilities and career advancement, subject to business needs and geographic mobility.