Analyst Clinical Data Management

Syngene International Limited; Bengaluru Urban; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Syngene International Limited is seeking an EDC Database Programmer in Bengaluru to design, develop, validate, and maintain clinical study databases within EDC systems. You will ensure data quality, protocol adherence, and timely study deliverables, while aligning with regulatory standards.

The role requires hands-on EDC programming experience, familiarity with CDISC standards, and collaboration with Data Management and Sponsors to support study setup and maintenance.

Qualifications

• Hands-on experience in EDC database programming within clinical trials.
• Exposure to Phase I–IV studies preferred.
• Ability to interpret study protocols and translate them into database specifications.

Responsibilities

• Design and develop clinical study databases within EDC systems per protocol and CRF specs.
• Configure eCRFs, visit structures, edit checks, derivations, and study workflows.
• Perform database validation and UAT to ensure functionality and compliance.
• Create and maintain edit check specs and test scripts.
• Support data cleaning by troubleshooting system-related queries.
• Implement mid-study updates and change control processes.
• Ensure compliance with GCP, CDISC, and 21 CFR Part 11.

Skills

EDC platforms

Analytical skills

Communication skills

Attention to detail

Deadline driven

Education

Bachelors in CS/IT

Masters in CS/IT

Tools

Medidata Rave

Inform

Veeva

Clinion

Job description

Job Description:

Date: 4 Apr 2026

Location:

IN

Division: Discovery Services

Job Description

Job Title: EDC Database Programmer

Job Location: Bangalore

Department: Clinical Data Management

About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.

At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit

Mandatory expectation for all roles as per Syngene safety guidelines

• Overall adherence to safe practices and procedures of oneself and the teams aligned
• Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards
• Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
• Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
• Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
• Compliance to Syngene’ s quality standards at all times
• Hold self and their teams accountable for the achievement of safety goals
• Govern and Review safety metrics from time to time

Core Purpose of the Role:

To design, develop, validate, and maintain clinical study databases within EDC systems, ensuring data quality, protocol compliance, and timely study deliverables in alignment with regulatory and organizational standards.

Role Accountabilities

• Design and develop clinical study databases within EDC systems as per protocol and CRF specifications.
• Configure eCRFs, visit structures, edit checks, derivations, and study workflows.
• Perform database validation and execute UAT to ensure system functionality and compliance.
• Create and maintain edit check specifications and test scripts.
• Support data cleaning activities by troubleshooting and resolving system-related queries.
• Implement mid-study updates, amendments, and change control processes.
• Ensure compliance with GCP, CDISC standards, and 21 CFR Part 11 requirements.
• Maintain study documentation including build documents, validation records, and audit trails.
• Collaborate with Data Management, Biostatistics, Clinical Operations, and Sponsors for study setup and maintenance.
• Support database lock activities and assist in system integrations (e.g., ePRO, IWRS, laboratory data).

Leadership Capabilities

• Demonstrates accountability and ownership of assigned studies.
• Proactively communicates risks and challenges to stakeholders.
• Works collaboratively within cross-functional teams.
• Shows willingness to learn and adapt to new systems and processes.
• Contributes positively to team performance and timelines.

Syngene Values

• Excellence
• Integrity
• Professionalism

Specific requirements for this role

• Experience
• Hands‑on experience in EDC database programming within clinical trials.
• Experience working on Phase I–IV studies preferred.
• Exposure to database build, testing, and maintenance activities.
• Demonstrated Capability
• Ability to interpret study protocols and translate them into database specifications.
• Experience in creating edit checks and validation rules.
• Capability to manage multiple tasks within defined timelines.
• Basic understanding of CDISC standards and regulatory compliance (GCP).
• Education
• Bachelor’s/master’s degree in: Computer Science/Information Technology
• Training in GCP, CDISC, or clinical data management is an added advantage

Looking for experienced candidates in Clinical Data Management or EDC Programming.

Skills And Capabilities

• Proficiency in EDC platforms (e.g., Medidata Rave, Inform, Veeva, Clinion or equivalent).
• Strong analytical and problem‑solving skills.
• Good written and verbal communication skills.
• Attention to detail and commitment to data quality.
• Ability to work in a deadline‑driven environment.

Education

• Bachelor’s/master’s degree in: Computer Science/Information Technology
• Training in GCP, CDISC, or clinical data management is an added advantage
• Certification in Clinical Data Management or EDC systems (preferred).

Equal Opportunity Employer

It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Requirements: