Senior Clinical Data Coordinator (CDC) – Bangalore, India
Location: Bangalore, India
Work Model: Office-Based or Remote
Job Type: Full-Time
Job Requisition ID: JR142366
Industry: Clinical Research / Clinical Data Management
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking an experienced Senior Clinical Data Coordinator (CDC) to join our dynamic team. This role is central to ensuring data integrity and accuracy across clinical trials, contributing to the development of innovative therapies and enhancing patient outcomes.
Role Overview
As a Senior Clinical Data Coordinator at ICON, you will manage, analyze, and reconcile clinical trial data, ensuring compliance with regulatory standards and high-quality data delivery. You will provide expertise in clinical data management, mentor junior staff, and collaborate with cross-functional teams to streamline data processes throughout the trial lifecycle.
Key Responsibilities
Develop, maintain, and execute detailed data management plans and documentation in compliance with ICH-GCP and other regulatory guidelines.
Identify, track, and resolve data discrepancies to ensure high-quality and accurate clinical trial datasets.
Collaborate with clinical operations, biostatistics, and other cross-functional teams to implement data management strategies tailored to individual studies.
Review and process data queries, coordinate with investigative sites, and ensure timely resolution of data issues.
Support project documentation, including filing, archiving, and regulatory submissions, maintaining inspection-ready records.
Mentor and guide junior data coordinators in data reconciliation, coding, cleaning, and quality control procedures.
Contribute to continuous improvement initiatives for data management processes and system workflows.
Required Experience & Skills
Bachelor’s degree in Life Sciences, Healthcare, or a related field; advanced degree preferred.
5+ years of experience in clinical data management within pharmaceutical, biotechnology, or CRO environments.
Strong proficiency with clinical data management systems (e.g., Medidata, Oracle RDC, or equivalent).
Knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
Excellent analytical, organizational, and problem-solving skills with strong attention to detail.
Effective communication and collaboration skills for working with global cross-functional teams.
Ability to manage multiple tasks in a fast-paced and structured clinical trial environment.
What ICON Offers
Competitive salary and global career growth opportunities.
Comprehensive benefits including health insurance, retirement planning, life assurance, and wellness programs.
Access to professional development, training, and mentoring opportunities.
An inclusive and diverse work culture that values innovation, operational excellence, and work-life balance.
ICON is committed to creating a workplace free from discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, gender, religion, disability, or other protected status.
This is an excellent opportunity for experienced clinical data professionals to advance their career while contributing to high-impact global clinical trials. Apply now to join ICON’s Bangalore team.
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