Location: Chennai, India (Office with Flex)
Job Type: Full-Time
Company: ICON plc
Job ID: JR142313
Experience Required: Minimum 5 Years (Not suitable for freshers)
About the Company
ICON plc is a globally recognized healthcare intelligence and clinical research organization driving innovation in drug development. With a strong presence across global markets, ICON partners with pharmaceutical, biotechnology, and medical device companies to accelerate clinical trials and deliver life-changing therapies.
Job Overview
The Clinical Data Coordinator II plays a crucial role in clinical data management by supporting the design, maintenance, and validation of clinical trial data systems. This role requires expertise in handling complex datasets, ensuring data integrity, and collaborating with cross-functional teams to support high-quality clinical research outcomes.
Key Responsibilities
Support the Data Management Study Lead in maintaining eCRFs, Data Validation Specifications, and study-specific procedures
Perform reconciliation of clinical and third-party data in accordance with edit checks and data review plans
Monitor, track, and communicate study progress, metrics, and deliverables to stakeholders
Address data-related queries and recommend effective resolution strategies
Identify root causes of data discrepancies and implement corrective actions
Ensure accuracy, completeness, and consistency of clinical trial data
Collaborate with clinical data scientists, project teams, and functional leadership
Required Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related healthcare field
Minimum 5 years of experience in Clinical Data Management
Strong understanding of clinical trial data workflows and processes
Hands-on experience with data management systems such as Medidata, Oracle RDC, or similar platforms
Knowledge of regulatory standards including ICH-GCP guidelines
Excellent analytical, problem-solving, and communication skills
Ability to work efficiently in a fast-paced, deadline-driven environment
Preferred Skills
Experience in handling multi-source clinical data reconciliation
Strong attention to detail with a proactive approach to data quality management
Ability to collaborate across global teams and stakeholders
Compensation and Benefits
Competitive salary aligned with industry standards
Comprehensive health insurance coverage for employees and families
Retirement and financial planning benefits
Global Employee Assistance Program for mental health and well-being support
Flexible work policies supporting work-life balance
Additional country-specific benefits such as childcare support, gym memberships, and travel benefits
Work Culture and Inclusion
ICON plc promotes an inclusive, diverse, and performance-driven work culture. The organization is committed to equal employment opportunities and provides a workplace free from discrimination and harassment. All qualified candidates are encouraged to apply irrespective of background.
Important Note for Applicants
This role requires prior hands-on experience in clinical data management. Freshers are advised to apply for entry-level roles such as Clinical Data Coordinator I, Clinical Data Associate, or Clinical Research Assistant positions to build foundational experience.
How to Apply
Interested candidates can apply through the official careers portal of ICON plc. For more verified global clinical research and pharmacovigilance job opportunities, visit ThePharmaDaily.com.
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