Data Manager (Expert in Programming & developing EDC systems) in India at Jobgether

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Data Manager (Expert in Programming & developing EDC systems) in India.

This role sits at the core of clinical data operations, ensuring the accuracy, integrity, and reliability of clinical trial data across complex studies. You will work within a highly collaborative, international environment supporting oncology and rare disease research programs that directly contribute to patient outcomes. The position combines technical expertise in EDC systems with hands-on clinical data management responsibilities across the full study lifecycle. You will play a key role in building, validating, and maintaining clinical databases while ensuring smooth data flow between multiple vendors and systems. This is a detail-oriented and impact-driven role where precision, compliance, and problem-solving are essential. You will collaborate closely with study teams, contribute to process improvements, and support high-quality data delivery for global clinical trials. The environment values autonomy, ownership, and continuous learning within a fast-evolving research landscape.

• Support end-to-end clinical data management activities from study start-up through database lock, ensuring high-quality and compliant data delivery.
• Perform validation of EDC systems, edit checks, SAS programs, and related data management reports and outputs.
• Build, test, and maintain clinical databases, including user acceptance testing and specification development for EDC systems.
• Manage EDC user accounts and ensure proper system access and functionality across studies.
• Oversee data cleaning activities including query management, SAE reconciliation, lab data tracking, and vendor data reconciliation.
• Perform or support data entry, medical coding, and review of study data as required.
• Generate and review study metrics, identify risks or roadblocks, and escalate issues appropriately to ensure timely resolution.
• Support database close-out activities, including final reconciliations, query resolution, and study reporting for database lock.

• Bachelor’s degree in Life Sciences, Computer Science, or a related scientific discipline.
• 4–8 years of experience in clinical data management within a pharmaceutical company, CRO, or similar regulated environment.
• Strong expertise in EDC systems, clinical database design, validation processes, and data cleaning activities.
• Solid understanding of clinical trial processes, data standards, and regulatory compliance requirements.
• Experience with SAS, edit checks, and data validation processes is highly desirable.
• Strong analytical mindset with excellent attention to detail and problem-solving skills.
• Ability to manage multiple studies simultaneously with minimal supervision.
• Effective communication skills and ability to work in cross-functional, international teams.

• International and collaborative work environment with global project exposure.
• Strong emphasis on work-life balance and employee well-being.
• Training and continuous career development opportunities.
• Inclusive and diverse workplace culture with equal opportunity principles.
• Opportunity to work remotely or across European locations (depending on role setup).
• Supportive team culture focused on knowledge sharing and professional growth.
• Engagement in meaningful clinical research contributing to oncology and rare disease advancements.