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 setting.

Experience with sponsor-facing projects is an added advantage.

Location: Flexible

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

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