Programmer Analyst I (Clinical data managers / database designers) in India at Jobgether

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Programmer Analyst I (Clinical Data Managers / Database Designers) in India.

You will join a global clinical research and data operations environment where you will contribute to the design, programming, and maintenance of clinical trial databases that support life-saving therapies. This role sits at the intersection of clinical data management and technical programming, focusing on interpreting study protocols and translating them into functional database structures and edit checks. You will work on multiple concurrent clinical studies using industry-standard EDC tools while ensuring high data quality, regulatory compliance, and timely delivery. The environment is highly collaborative and detail-oriented, involving close interaction with data managers, programmers, and study teams across global projects. You will also contribute to the development of data visualizations, validation processes, and submission-ready deliverables. This is a strong opportunity for professionals looking to grow into clinical programming while working in a regulated, impact-driven healthcare domain.

• Perform independent programming activities across multiple clinical studies using EDC systems such as Medidata Rave or Veeva.
• Interpret clinical study protocols and data management specifications to design and build clinical databases and edit checks.
• Develop and validate database structures, datasets, and programming specifications aligned with CDISC and client standards.
• Create and maintain submission deliverables including annotated CRFs, Define XML/PDFs, and Reviewer’s Guides.
• Build and support data quality checks, listings, protocol deviation reports, and post-production database enhancements.
• Develop visual analytics dashboards using tools such as Spotfire or Tableau to support study insights.
• Ensure compliance with GCP guidelines, SOPs, and regulatory requirements in all programming activities.
• Perform database reconciliation, quality checks, and validation of clinical programming outputs.
• Collaborate with cross-functional teams and communicate data issues to data management stakeholders.
• Support training and mentoring of junior team members on EDC tools and programming practices.

• 4–7 years of relevant experience in clinical data management, database programming, or clinical systems support.
• At least 2 years of hands-on experience in protocol interpretation and clinical study build activities.
• Strong understanding of clinical trial processes, data management, and biometrics principles.
• Experience working with EDC tools such as Medidata Rave and/or Veeva Systems.
• Familiarity with clinical programming deliverables such as edit checks, listings, and database design documentation.
• Knowledge of CDISC standards and regulatory expectations in clinical research environments.
• Experience with data visualization tools such as Spotfire or Tableau is a plus.
• Strong analytical, problem-solving, and attention-to-detail skills.
• Ability to manage multiple projects independently and meet tight deadlines.
• Excellent communication, teamwork, and stakeholder coordination abilities.
• Bachelor’s degree in Life Sciences, Health Sciences, IT, or related field preferred.

• Fully remote work arrangement with flexibility across India.
• Opportunity to work on global clinical trials impacting life-saving therapies.
• Exposure to advanced EDC platforms and clinical data programming tools.
• Career development in clinical programming, data management, and analytics.
• Work within a highly regulated, quality-driven healthcare research environment.
• Collaborative international team environment with cross-functional exposure.
• Structured processes aligned with global regulatory and compliance standards.
• Continuous learning and upskilling opportunities in clinical systems and analytics.