Senior Clinical Data Coordinator

About IQVIA

IQVIA stands as a premier global entity offering sophisticated analytics, technology solutions, and contract research services tailored to the life sciences sector. Created by merging IMS Health and Quintiles, the company harnesses human data science to innovate clinical development and commercialization, accelerating advancements in healthcare outcomes. Leveraging the IQVIA CORE, the company provides unmatched insights combining large-scale data analytics, groundbreaking technology, and deep domain expertise. Operating in over 100 countries and boasting a workforce exceeding 86,000 employees, IQVIA has earned recognition on FORTUNE's 2026 list of "World's Most Admired Companies." Joining IQVIA offers a platform to grow professionally while contributing to improved human health outcomes.

Key Responsibilities

• Oversee and manage comprehensive Clinical Data Management (CDM) operations throughout the lifecycle of clinical studies.
• Engage in study initiation activities, such as reviewing Case Report Forms (CRFs), performing User Acceptance Testing (UAT), and validating databases.
• Conduct continuous data assessments including discrepancy resolution and data cleaning during study execution.
• Collaborate effectively with cross-disciplinary teams like Clinical Operations, Biostatistics, Programming, and Data Management stakeholders.
• Guarantee high-quality data management compliant with standards and adhere to project timelines.
• Support the database lock process and other close-out deliverables at study conclusion.
• Identify and recommend enhancements to improve data management procedures and adopt best practices.

Qualifications and Requirements

• At least 4.5 years of pertinent experience in Clinical Data Management.
• Minimum 5 years working experience covering end-to-end CDM processes.
• Practical knowledge of Medidata Rave EDC platform.
• Comprehensive understanding of clinical trial phases, including Start-Up, Conduct, and Close-Out stages.
• Proficient in UAT, database lock, query handling, data cleaning, and familiarity with CDISC standards.
• Ability to adapt to shift-based work schedules based on business needs.
• Excellent communication capabilities and strong stakeholder coordination skills.
• Preferred experience includes involvement in sponsor-facing projects and an understanding of regulatory requirements governing clinical trials.

Additional Information

The role is based in Bangalore Rural, India, requiring flexibility to work in rotational shifts as demanded by operational requirements. Candidates holding any graduate degree are eligible to apply for this position.