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Tier-1 brand, mid-level experience, and Bangalore metro increase applicant competition.
Clinical trial systems and GxP requirements strongly limit cross-industry transferability.
Requires 2–3 years pharma clinical data systems experience and GxP compliance, making filters strict.
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Manage user access, roles, and configuration across clinical data management systems (EDC, eCOA, Veeva) to support global clinical trials.
Support end-users through incident resolution and system-related queries, ensuring compliance with SOPs, GCP, GDP, and GxP.
Collaborate with cross-functional and global teams to deliver compliant solutions and contribute to process improvements in clinical data operations.
Bachelor's or Master's degree in Life Sciences, Computer Science, Information Technology, Clinical Information Management, or related field.
2–3 years of experience in pharmaceutical, biotechnology, clinical research, or healthcare industry.
Experience with Clinical Data Management systems, user access management, or related platforms.
Knowledge of clinical trial processes and GxP regulatory requirements.
Strong operational focus on user access and system configuration within clinical data management environments.
Comfortable working in a structured, compliance-driven, global clinical trial setting involving vendor and cross-functional collaboration.
Experienced in managing clinical data systems and compliant documentation under regulated environments.