Experience Required: Minimum 4.5+ Years of Relevant Clinical Data Management Experience

Key Requirements:

Minimum 5 years of relevant experience in end-to-end Clinical Data Management (CDM).

Hands-on experience with Medidata Rave EDC.

Strong experience across the complete clinical trial lifecycle, including:

Study Start-Up

Study Conduct

Study Close-Out

Expertise in clinical data management activities from User Acceptance Testing (UAT) through Database Lock.

Willingness to work in shift-based environments as per business requirements.

Good understanding of CDISC standards, data review, query management, and data cleaning processes.

Key Responsibilities:

Manage and oversee end-to-end CDM activities for clinical studies.

Participate in study start-up activities, including CRF review, UAT, and database validation.

Perform ongoing data review, discrepancy management, and data cleaning throughout study conduct.





Coordinate with cross-functional teams, including Clinical Operations, Biostatistics, Programming, and Data Management stakeholders.

Ensure data quality, compliance, and adherence to project timelines.

Support database lock activities and study close-out deliverables.

Identify process improvement opportunities and contribute to best practices within Data Management.

Preferred Skills:

Strong knowledge of clinical trial processes and regulatory requirements.

Excellent communication and stakeholder management skills.

Ability to work independently in a fast-paced and global environment.

Experience with sponsor-facing projects is an added advantage.

Location: Flexible

Shift: Versatile/Willing to work in rotational shifts as required.

📌 Senior Clinical Data Coordinator (Bangalore Rural)
🏢 Iqvia
📍 Bangalore Rural