Clinical Data Manager I – Bengaluru, India (Hybrid)
Job Type: Full-Time | Experience Required: 1+ Year | Location: Bengaluru, Karnataka, India
About Excelya
Excelya is a leading, ambitious clinical research organization (CRO) driven by audacity, care, and energy. Our inclusive, collaborative culture encourages innovation, personal growth, and professional development. As a Clinical Data Manager I, you will join a dynamic team in Bengaluru and contribute directly to cutting-edge clinical research projects that impact patient outcomes globally.
At Excelya, you’ll work in an environment that combines scientific excellence with operational expertise, offering exposure to diverse projects across full-service, functional service provider, and consulting models.
Role Overview
As a Clinical Data Manager I, you will play a critical role in clinical data collection, management, and quality control. You will ensure accuracy, compliance, and integrity of clinical trial data, supporting study teams throughout the trial lifecycle from start-up to closeout.
This position is ideal for individuals with hands-on experience in clinical data management who are ready to contribute to a collaborative, growth-oriented environment.
Key Responsibilities
Manage and review clinical trial data to ensure accuracy, consistency, and regulatory compliance.
Oversee electronic Case Report Form (eCRF) design, data review, and clinical database management.
Ensure clinical data flow aligns with study protocols and timelines.
Collaborate with cross-functional teams, including clinical operations, biostatistics, and regulatory affairs, to support trial deliverables.
Maintain compliance with ICH GCP, FDA, EU, and other relevant guidelines throughout the study lifecycle.
Identify data discrepancies, generate queries, and facilitate timely resolutions.
Support study teams during trial start-up, maintenance, and closeout activities.
Document processes and updates to maintain a clear audit trail for regulatory inspection readiness.
Required Qualifications & Skills
Experience: 1+ year in clinical data management or equivalent combination of education, training, and experience.
Education: Bachelor’s degree in a scientific discipline preferred.
Strong knowledge of ICH GCP and applicable regulatory guidelines (FDA, EU, ICH).
Experience with clinical trial databases, eCRF design, and clinical data review.
Understanding of clinical trial lifecycle and associated workflows.
Excellent written and verbal English communication skills.
Strong attention to detail, problem-solving abilities, and organizational skills.
Preferred Qualifications
Exposure to global clinical trials and multi-country study coordination.
Familiarity with data management systems, CDISC standards, and data cleaning processes.
Previous experience in a CRO environment or clinical operations.
Why Excelya?
Join a young, ambitious, and growing CRO with over 900 employees across Europe and India.
Contribute to diverse projects with exposure to full-service, functional service provider, and consulting models.
Work alongside experts in clinical research and enhance operational, scientific, and human knowledge.
Thrive in an inclusive, equitable, and collaborative environment that values curiosity, creativity, and professional growth.
Competitive environment fostering learning, career development, and impact on patient outcomes.
Apply Today
If you are ready to excel in clinical data management, ensure data integrity, and contribute to innovative clinical trials, join Excelya as a Clinical Data Manager I and be part of a team shaping the future of healthcare.
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