Clinical Data Coordinator II (CDC II)
Locations: Chennai | Bangalore | Trivandrum, India
Work Model: Office with Flex
Employment Type: Full-Time
Industry: Clinical Data Management | Clinical Research | CRO
Company: ICON plc
Job Overview
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a skilled Clinical Data Coordinator II (CDC II) to support end-to-end clinical data management activities across global clinical trials. This role plays a key part in ensuring high-quality clinical data, regulatory compliance, and efficient study execution within a fast-paced CRO environment.
The position is ideal for professionals with strong experience in clinical data management systems, data reconciliation, and cross-functional collaboration, looking to grow within a globally recognized organization.
Key Responsibilities
Support the Data Management Study Lead in maintaining electronic Case Report Forms (eCRFs), Data Validation Specifications, and Study-Specific Procedures.
Perform clinical and third-party data reconciliation in accordance with edit specifications and data review plans.
Track, monitor, and communicate study-level and task-level metrics to Clinical Data Scientists, project teams, and functional leadership.
Address data-related queries, identify trends, and recommend effective solutions to data issues.
Conduct root cause analysis to systematically resolve recurring data discrepancies and quality concerns.
Ensure data management activities comply with ICH-GCP, regulatory standards, and internal SOPs.
Collaborate with cross-functional teams to support timely database cleaning and study milestones.
Required Qualifications & Experience
Education:
Bachelor’s degree in Life Sciences, Healthcare, Pharmacy, Biotechnology, or a related discipline.
Experience:
Minimum 5 years of relevant experience in Clinical Data Management within a CRO, pharmaceutical, or biotechnology organization.
Hands-on experience supporting data cleaning, reconciliation, and study-level data management activities.
Technical & Professional Skills:
Intermediate to advanced knowledge of clinical data management processes across the clinical trial lifecycle.
Experience with EDC systems such as Medidata Rave, Oracle RDC, or equivalent platforms.
Strong understanding of clinical trial data standards and regulatory guidelines (ICH-GCP knowledge preferred).
Excellent attention to detail with the ability to work efficiently in a deadline-driven environment.
Strong written and verbal communication skills with proven ability to collaborate across global teams.
Why Join ICON
ICON offers a collaborative, inclusive, and performance-driven work environment where employees are empowered to grow their careers. The organization provides competitive compensation, robust health and wellness benefits, flexible work arrangements, and continuous learning opportunities.
Benefits Overview
Competitive salary and performance-based incentives
Comprehensive health insurance coverage for employees and families
Generous annual leave and holiday entitlements
Retirement and long-term financial planning benefits
Global Employee Assistance Program (TELUS Health)
Life assurance and optional country-specific benefits
Focus on employee well-being and work-life balance
Equal Opportunity Statement
ICON is an equal opportunity employer committed to fostering a diverse and inclusive workplace. All qualified applicants will receive equal consideration for employment without regard to race, religion, gender, sexual orientation, disability, or protected veteran status. Reasonable accommodations are available throughout the recruitment process.
Apply Now
If you are an experienced Clinical Data Management professional seeking to advance your career with a global CRO, apply today and become part of ICON’s mission to advance and improve patients’ lives worldwide.
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