Clinical Data Coordinator II Jobs at ICON plcII in India for clinical data management roles with flexible office options.
ICON plc, a globally recognized healthcare intelligence and clinical research organization, is hiring for the position of Clinical Data Coordinator II (CDC II) in India. This is a full-time opportunity for experienced clinical data management professionals looking to work in a flexible office environment while contributing to innovative clinical research projects.
The role is open across multiple Indian locations including Chennai, Bangalore, and Trivandrum. ICON is known for its inclusive work culture, strong career development framework, and commitment to advancing the future of clinical development worldwide. Clinical Data Coordinator II Jobs at ICON plc
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies throughout the entire clinical development lifecycle. With a presence in over 40 countries, ICON delivers integrated solutions that enhance trial efficiency, data quality, and patient outcomes.
The organization is driven by innovation, scientific excellence, and a strong people-first culture. ICON emphasizes inclusion, diversity, and belonging, ensuring that employees from all backgrounds feel valued and supported. Its global teams work collaboratively to bring life-changing therapies to patients faster and more efficiently. Clinical Data Coordinator II Jobs at ICON plc
Working at ICON means being part of an organization that combines global reach with local expertise, offering employees long-term career growth, learning opportunities, and meaningful work in clinical research.
Job Details
Job Title: Clinical Data Coordinator II (CDC II)
Job Requisition ID: JR141730
Employment Type: Full-time
Work Mode: Office with Flex
Locations:
- Chennai, India
- Bangalore, India
- Trivandrum, India
- Application Deadline: January 23, 2026
Job Description
ICON is seeking a skilled and detail-oriented Clinical Data Coordinator II to join its Clinical Data Management team. In this role, you will support the design, execution, and data quality of clinical trials across various therapeutic areas. Clinical Data Coordinator II Jobs at ICON plc
As a CDC II, you will work closely with Data Management Study Leads, Clinical Data Scientists, and cross-functional project teams. Your responsibilities will focus on maintaining electronic case report forms (eCRFs), managing clinical and third-party data reconciliation, and ensuring that clinical trial data meets quality, regulatory, and operational standards.
This position is ideal for professionals with strong experience in clinical data management who are comfortable working in a fast-paced, global clinical research environment and who enjoy solving complex data-related challenges. Clinical Data Coordinator II Jobs at ICON plc
Key Responsibilities
- Support the Data Management Study Lead in maintaining eCRFs, Data Validation Specifications, and study-specific procedures
- Perform clinical and third-party data reconciliation according to edit specifications and data review plans
- Track, analyze, and communicate study and task metrics to Clinical Data Scientists, project teams, and functional management
- Address data-related queries and recommend appropriate solutions in collaboration with stakeholders
- Identify root causes of data discrepancies and implement systematic resolutions
- Ensure accuracy, completeness, and consistency of clinical trial data
- Contribute to continuous improvement of data management processes
- Maintain compliance with internal SOPs, regulatory guidelines, and industry standards
Clinical Data Coordinator II Jobs at ICON plc
Skills / Qualifications
Educational Qualifications
- Bachelor’s degree in Life Sciences, Healthcare, or a related scientific discipline
Experience Requirements
- Minimum 5 years of relevant experience in Clinical Data Management activities
- Prior experience working within pharmaceutical, biotechnology, or CRO environments
Technical and Professional Skills
- Intermediate to advanced knowledge of clinical data management processes
- Familiarity with clinical data management systems such as Medidata, Oracle RDC, or similar platforms
- Strong understanding of data validation, reconciliation, and data cleaning activities
- Knowledge of regulatory guidelines and standards such as ICH-GCP is an advantage
- High attention to detail with strong analytical and problem-solving skills
- Ability to work effectively in a fast-paced, deadline-driven environment
- Excellent written and verbal communication skills
- Proven ability to collaborate with cross-functional and global teams
Clinical Data Coordinator II Jobs at ICON plc
Benefits / Perks
ICON offers a comprehensive and competitive benefits package designed to support employee well-being, financial security, and work-life balance. Clinical Data Coordinator II Jobs at ICON plc
Key benefits include:
- Competitive salary aligned with industry standards
- Multiple annual leave entitlements
- Health insurance plans tailored to individual and family needs
- Retirement and long-term savings plans
- Life assurance coverage
- Global Employee Assistance Programme (TELUS Health) with 24/7 access to a global network of professionals
- Flexible, country-specific benefits such as childcare support, fitness and gym discounts, subsidized travel options, and health assessments
- Flexible work arrangements supporting work-life balance
Benefits may vary by location and are designed to meet local market expectations while maintaining global consistency.
Clinical Data Coordinator II Jobs at ICON plc
Why You Should Join
Joining ICON means becoming part of a global organization that is shaping the future of clinical research. Employees at ICON are encouraged to grow professionally, take ownership of their work, and contribute to meaningful projects that improve patient lives.
ICON’s inclusive culture ensures equal opportunities for all employees, with strong policies against discrimination and harassment. The organization actively supports diversity, accessibility, and belonging, creating a workplace where everyone can thrive.
If you are looking to advance your career in clinical data management while working on impactful global trials, ICON provides the platform, resources, and support to help you succeed. Clinical Data Coordinator II Jobs at ICON plc
FAQs
Is this a full-time role?
Yes, the Clinical Data Coordinator II position is a full-time role.
Can I apply if I am unsure I meet all requirements?
Yes. ICON encourages candidates to apply even if they do not meet every listed requirement, as transferable skills and potential are valued.
What work model is offered for this role?
This role follows an office-with-flex model, allowing flexibility while maintaining collaboration.
Is prior CRO experience mandatory?
Relevant clinical data management experience is required; CRO experience is preferred but not mandatory.
Does ICON provide accommodation for candidates with disabilities?
Yes. ICON is committed to providing reasonable accommodations during the application process and employment.
Clinical Data Coordinator II Jobs at ICON plc
How to Apply
Interested candidates should apply online through the official ICON careers portal before January 23, 2026.
Current ICON employees should apply through the internal employee portal.
This is an excellent opportunity to join a globally respected clinical research organization and advance your career in clinical data management. Clinical Data Coordinator II Jobs at ICON plc
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