Syngene International Limited is hiring for Analyst Clinical Data Management jobs in Bangalore. The position is functionally described as an EDC Database Programmer within the Clinical Data Management department and is intended for experienced candidates with hands-on exposure to Clinical Data Management or EDC programming.

This is an excellent opportunity for Computer Science and Information Technology graduates with experience in clinical trials, EDC database programming, database builds, edit checks, validation, and study maintenance. Candidates with knowledge of Medidata Rave, Oracle InForm, Veeva, Clinion, GCP, CDISC, and 21 CFR Part 11 may be particularly relevant for the role.

Syngene published this vacancy on 23 August 2026 for its Bangalore operations. Interested candidates should review the eligibility requirements carefully and apply through Syngene’s official careers portal.

About Syngene International

Syngene International Limited is an innovation-led contract research, development and manufacturing organization providing integrated scientific services ranging from early discovery through commercial supply.

The organization works across research, development, manufacturing, and scientific services and emphasizes safety, integrity, quality, professionalism, and regulatory compliance.

Job Overview

Core Purpose of the Role

The EDC Database Programmer at Syngene will be responsible for designing, developing, validating, and maintaining clinical study databases within Electronic Data Capture systems.

The role focuses on ensuring clinical trial databases meet protocol requirements, maintain high data quality, comply with applicable regulatory standards, and support study deliverables throughout the clinical trial lifecycle.

Key Responsibilities

Candidates selected for the Syngene Clinical Data Management job in Bangalore may be responsible for:

• Designing and developing clinical study databases within EDC systems according to study protocols and CRF specifications.
• Configuring electronic Case Report Forms (eCRFs), visit structures, workflows, edit checks, and derivations.
• Performing database validation and executing User Acceptance Testing (UAT).
• Creating and maintaining edit-check specifications and associated test scripts.
• Supporting clinical data cleaning by investigating and resolving system-related issues.
• Implementing protocol amendments, mid-study database updates, and controlled changes.
• Ensuring database activities comply with GCP, CDISC standards, and 21 CFR Part 11 requirements.
• Maintaining database-build documentation, validation records, audit trails, and other study documentation.
• Collaborating with Clinical Data Management, Biostatistics, Clinical Operations, sponsors, and other stakeholders.
• Supporting clinical database lock activities.
• Assisting with integrations involving systems and external data sources such as ePRO, IWRS, and laboratory data.
• Maintaining data quality throughout study setup, maintenance, and database closeout.
• Identifying risks and communicating potential issues to relevant stakeholders.

Qualification

Candidates applying for the Syngene EDC Database Programmer vacancy should have:

Bachelor’s or Master’s degree in:

• Computer Science
• Information Technology

Additional training in the following areas is considered advantageous:

• Good Clinical Practice (GCP)
• CDISC
• Clinical Data Management
• EDC systems

Certification in Clinical Data Management or EDC systems is preferred but is not stated as mandatory.

Experience Required

Syngene is specifically looking for experienced candidates in Clinical Data Management or EDC Programming.

Applicants should ideally have:

• Hands-on experience in EDC database programming for clinical trials.
• Exposure to clinical database build, testing, and maintenance.
• Experience interpreting clinical study protocols.
• Experience developing edit checks and validation rules.
• Understanding of clinical trial database specifications.
• Experience managing multiple activities within project timelines.

Experience working on Phase I, Phase II, Phase III, or Phase IV clinical studies is preferred.

The employer has not specified an exact number of years of experience in the provided job description. Candidates should therefore assess their suitability based on relevant hands-on CDM or EDC programming experience.

EDC & Technical Skills Required

Candidates should have proficiency or practical exposure to EDC platforms such as:

• Medidata Rave
• Oracle InForm
• Veeva
• Clinion
• Equivalent clinical EDC platforms

Knowledge of the following concepts will also be valuable:

• EDC database programming
• eCRF development
• Edit checks
• Validation rules
• Database testing
• UAT
• Clinical data cleaning
• Database lock
• Clinical study protocols
• CDISC standards
• GCP
• 21 CFR Part 11
• Clinical data integrations
• Audit trails
• Change control

Skills and Capabilities

Syngene is looking for candidates who demonstrate:

• Strong analytical skills
• Problem-solving abilities
• Attention to detail
• Commitment to clinical data quality
• Written and verbal communication skills
• Ability to meet project deadlines
• Cross-functional collaboration
• Accountability and ownership
• Ability to identify and communicate risks
• Willingness to learn new technologies and processes

Who Should Apply?

This Syngene Clinical Data Management recruitment 2026 is particularly relevant for professionals currently working in roles such as:

EDC Database Programmer, Clinical Database Programmer, Clinical Data Management Analyst, EDC Programmer, Database Designer, Clinical Data Programmer, or similar clinical research technology roles.

Applicants with a Computer Science or Information Technology educational background and relevant clinical trial database experience should consider applying.

Can Freshers Apply?

The vacancy specifically states that Syngene is looking for experienced candidates in Clinical Data Management or EDC Programming.

Therefore, this should not be treated as a dedicated fresher vacancy. Candidates with relevant internships or training but no professional experience may apply at their discretion, but Syngene has explicitly indicated a preference for experienced applicants.

Safety and Compliance Responsibilities

Syngene places significant emphasis on workplace safety and compliance. Employees are expected to:

• Follow applicable safety procedures and SOPs.
• Maintain adherence to company quality standards.
• Complete mandatory data integrity, health, and safety training.
• Follow Environment, Health and Safety requirements.
• Maintain operational discipline.
• Demonstrate accountability for safety and quality objectives.

Syngene Values

Employees are expected to demonstrate alignment with Syngene’s core organizational values:

Excellence | Integrity | Professionalism

Salary

The official job advertisement does not disclose salary information.

Based on the role, Bangalore market conditions, required technical skills, and the requirement for experienced Clinical Data Management/EDC professionals, an indicative editorial estimate could be:

₹5,00,000 – ₹10,00,000 per year

Actual salary may vary substantially based on previous experience, EDC platform expertise, current compensation, interview performance, and Syngene’s internal compensation structure.

Note: This salary range is an editorial estimate and has not been announced by Syngene International Limited.

Why Consider This Syngene CDM Opportunity?

This role can provide relevant professional exposure to:

• Clinical study database development
• EDC programming
• eCRF configuration
• Database validation
• UAT and testing
• Clinical data management
• Regulatory compliance
• Cross-functional clinical research teams
• Phase I–IV clinical trials
• Database integrations and lock activities

Professionals interested in developing a career combining clinical research, data management, and technology may find the role particularly relevant.

How to Apply

Application Link