Senior Clinical Data Coordinator Jobs at ICON plc (CDC II) professionals in Bangalore and Chennai – Apply now for clinical research careers.
About ICON plc
ICON plc is a global leader in healthcare intelligence and clinical research. Headquartered in Dublin, ICON partners with major pharmaceutical, biotechnology, and medical device companies to advance clinical development and bring innovative treatments to market faster. With operations in more than 100 countries, ICON delivers full-service solutions across clinical trials, data analytics, regulatory support, and post-market surveillance. Senior Clinical Data Coordinator Jobs at ICON plc
The company is renowned for fostering an inclusive, collaborative, and innovative work culture, making it one of the most sought-after employers in the global clinical research industry. ICON’s mission is simple yet powerful — to shape the future of clinical development and improve patient outcomes worldwide. Senior Clinical Data Coordinator Jobs at ICON plc
If you’re passionate about data management and want to play a vital role in clinical trial success, this opportunity as Senior Clinical Data Coordinator (CDC II) could be your perfect next career move. Senior Clinical Data Coordinator Jobs at ICON plc
Position: Senior Clinical Data Coordinator (CDC II)
- Job Type: Full-time
- Work Type: Office or Home (Hybrid flexibility)
- Locations: Bangalore, Chennai – India
- Job Requisition ID: JR131289
About the Role
ICON plc is currently seeking a Clinical Data Coordinator II (CDC II) to join its Clinical Data Management team. In this role, you will be responsible for managing, validating, and analyzing clinical data to ensure accuracy, consistency, and integrity across clinical studies.
You will collaborate closely with cross-functional teams — including clinical operations, biostatistics, regulatory affairs, and project management — to deliver high-quality data outputs that meet both internal standards and regulatory requirements. Senior Clinical Data Coordinator Jobs at ICON plc
This position offers an excellent opportunity to gain exposure to global clinical trials, enhance your data management expertise, and contribute to life-changing medical research projects. Senior Clinical Data Coordinator Jobs at ICON plc
Key Responsibilities
As a Clinical Data Coordinator II, you will be responsible for a wide range of data management and coordination activities, including: Senior Clinical Data Coordinator Jobs at ICON plc
1. Study Data Management
- Assist the Data Management Study Lead (DMSL) in maintaining key study documents such as eCRF (Electronic Case Report Forms), Data Validation Specifications, and Study-Specific Procedures.
- Ensure accurate entry, validation, and reconciliation of clinical trial data from multiple sources.
- Monitor the consistency and completeness of data, identifying and resolving discrepancies.
2. Data Reconciliation and Review
- Manage and reconcile data across clinical and third-party sources as per the Edit Specifications and Data Review Plans.
- Perform quality checks on data to ensure compliance with study protocols and global data management standards.
- Collaborate with data scientists and statisticians to identify and correct data issues systematically.
3. Communication and Reporting
- Track and report on study status and key task metrics to the Clinical Data Scientist, Project Team, and Functional Management.
- Prepare detailed reports on data issues, root cause analyses, and resolution progress.
- Communicate effectively with stakeholders across departments and countries to ensure timely project delivery.
4. Issue Resolution and Documentation
- Address all data-related queries from internal and external stakeholders.
- Recommend solutions for complex data issues and ensure documentation of data management processes.
- Maintain version control and compliance for all data-related documentation.
- Senior Clinical Data Coordinator Jobs at ICON plc
Candidate Profile
To succeed as a Senior CDC / CDC II at ICON plc, candidates should meet the following qualifications and skill requirements: Senior Clinical Data Coordinator Jobs at ICON plc
Educational Qualification:
- Bachelor’s degree in Life Sciences, Healthcare, Pharmacy, Biotechnology, or related fields.
- A Master’s degree in Clinical Research or Data Management is a plus but not mandatory.
Experience:
- 2 to 4 years of experience in Clinical Data Management (CDM) within the pharmaceutical, biotechnology, or CRO industry.
- Experience in global clinical trials and exposure to multiple therapeutic areas is an advantage.
Technical Skills:
- Intermediate knowledge of clinical data management systems such as Medidata Rave, Oracle RDC, or similar platforms.
- Proficiency in Microsoft Office tools, especially MS Excel for data analysis and reporting.
- Familiarity with Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS).
- Understanding of data validation procedures, query management, and database lock processes.
Knowledge Requirements:
- Good understanding of ICH-GCP (International Council for Harmonisation – Good Clinical Practice) guidelines.
- Awareness of CDISC standards (Clinical Data Interchange Standards Consortium).
- Knowledge of regulatory data management requirements (FDA, EMA, etc.).
- Senior Clinical Data Coordinator Jobs at ICON plc
Behavioral Competencies
ICON values professionals who demonstrate strong interpersonal and organizational skills. Ideal candidates should possess:
- Excellent time management and multitasking abilities.
- A proactive, solution-oriented mindset with strong attention to detail.
- Ability to thrive in fast-paced and multicultural environments.
- Strong communication skills — both verbal and written — with the ability to collaborate across cross-functional teams.
- A strong sense of accountability and the ability to work independently when required.
Why Join ICON plc?
ICON’s success depends on the quality, dedication, and innovation of its people. The company has built a culture that values performance, learning, and inclusion.
Here’s what makes ICON an employer of choice in the clinical research industry:
1. Competitive Compensation
ICON offers competitive salary packages that reflect your skills and experience, along with annual performance-linked incentives.
2. Health and Wellness Benefits
- Comprehensive health insurance for you and your family.
- Access to TELUS Health – Global Employee Assistance Programme, offering 24-hour support from a network of over 80,000 professionals worldwide.
- Wellness programs and health assessments to promote work-life balance.
3. Retirement and Financial Planning
- Competitive retirement benefits to help you plan confidently for your future.
- Country-specific financial assistance programs, including provident fund and pension schemes.
4. Work-Life Balance
- Flexible work options, including hybrid and remote models.
- Generous annual leave entitlements and flexible work hours.
- Country-specific perks like childcare vouchers, gym memberships, and commuting benefits.
5. Learning and Development
- Continuous professional development programs and access to ICON University for skill enhancement.
- Opportunities for global collaboration and internal mobility across departments and regions.
6. Diversity and Inclusion
At ICON, diversity and belonging are integral to the company culture. The organization is committed to providing an inclusive and discrimination-free workplace.
All applicants are considered regardless of gender, ethnicity, religion, disability, or veteran status. Senior Clinical Data Coordinator Jobs at ICON plc
How to Apply for Senior CDC / CDC II Jobs at ICON plc
If you’re ready to advance your career in clinical data management, follow these steps to apply: Senior Clinical Data Coordinator Jobs at ICON plc
- Visit the Official ICON Careers Page:
Go to careers.iconplc.com and search for “Senior CDC / CDC II – India”. - Select Your Preferred Location:
Choose Bangalore or Chennai, depending on your preference for office or hybrid work options. - Prepare Your Resume:
Update your resume to highlight your data management experience, software proficiency, and clinical research knowledge. - Submit Your Application:
Click on “Apply” and complete the online form with your details, qualifications, and work experience. - Follow Up:
If shortlisted, you will receive an email for the next steps, including assessments or interviews.
Final Thoughts
The Senior CDC / CDC II role at ICON plc is an outstanding opportunity for professionals looking to enhance their expertise in clinical data management. With ICON’s global presence, structured career growth, and commitment to innovation, you can build a rewarding and impactful career in the field of clinical research. Senior Clinical Data Coordinator Jobs at ICON plc
If you’re passionate about clinical trials, data accuracy, and patient safety — apply now and become part of a company that’s redefining the future of healthcare innovation. Senior Clinical Data Coordinator Jobs at ICON plc
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