ICON plc Hiring for Clinical Data Coordinator II
Job Role: Clinical Data Coordinator II (CDC II)
Location: Bangalore | Trivandrum | Chennai
Experience Required: 1–3 Years
Education: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
Mode of Application: Online
Verified Job
ICON plc, a globally recognized leader in clinical research and healthcare intelligence, is inviting applications for the position of Clinical Data Coordinator II (CDC II) at its India offices. This opportunity is open to life sciences graduates with 1–3 years of experience in clinical data management.
For candidates aspiring to build a strong career in the clinical research field, this is a golden opportunity to work with a company known for innovation, diversity, and global impact in the pharmaceutical and biotech industries. ICON plc Hiring for Clinical Data Coordinator II
About ICON plc
ICON plc is a global contract research organization (CRO) that specializes in clinical development and data services for pharmaceutical, biotechnology, and medical device companies. Headquartered in Dublin, Ireland, ICON operates across six continents and serves clients in over 90 countries.
With a sharp focus on clinical data excellence, ICON helps sponsors accelerate drug development, optimize regulatory submissions, and bring life-saving therapies to patients faster. The company is known for a high-performance culture, a commitment to employee growth, and a deep-rooted belief in ethical and quality-driven work. ICON plc Hiring for Clinical Data Coordinator II
Job Overview – Clinical Data Coordinator II
Job Title: Clinical Data Coordinator II
Department: Clinical Data Management
Location: Bangalore, Trivandrum, Chennai
Experience Level: 1–3 Years
Educational Qualification: Degree in Life Sciences or related field
As a Clinical Data Coordinator II, your primary responsibility will be to ensure the integrity, quality, and accuracy of clinical trial data collected from investigational sites and third-party vendors. You will work closely with data managers, programmers, biostatisticians, and project teams to support end-to-end data activities. ICON plc Hiring for Clinical Data Coordinator II
Key Responsibilities
- Assist the Data Management Study Lead in study setup, including the development and review of eCRF designs, Data Validation Specifications, and Data Management Plans.
- Handle third-party data reconciliation and perform query management based on predefined edit check specifications.
- Ensure timely and accurate data cleaning, discrepancy resolution, and data review throughout the study lifecycle.
- Track study progress and provide status reports and metrics to stakeholders and team leads.
- Identify the root cause of data issues, propose corrective actions, and drive implementation to prevent reoccurrence.
- Support database lock processes and regulatory submission activities.
- Ensure compliance with ICH-GCP, CDISC, and SOPs throughout all data handling stages.
- ICON plc Hiring for Clinical Data Coordinator II
Desired Candidate Profile
Essential Qualifications:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or equivalent discipline.
- 1 to 3 years of experience in Clinical Data Management within a CRO, pharmaceutical company, or biotech.
- Hands-on experience with clinical data management tools like Medidata RAVE, Oracle RDC, or InForm.
- Good understanding of clinical trial phases, protocol structure, and CRF design.
- Familiarity with CDM processes, including query resolution, coding, SAE reconciliation, and external data handling.
Key Competencies:
- Strong attention to detail and analytical thinking.
- Ability to work independently and manage multiple priorities in a fast-paced environment.
- Effective communication skills – verbal and written.
- Sound knowledge of ICH-GCP guidelines and regulatory requirements is an added advantage.
- Proven ability to work in a collaborative team across functions and geographies.
Why Choose ICON plc?
ICON is not just a workplace – it’s a platform for career growth, skill enhancement, and international exposure. Here’s what makes ICON an attractive employer for clinical research professionals: ICON plc Hiring for Clinical Data Coordinator II
- Global Exposure: Be part of a company involved in multi-country, high-impact clinical studies.
- Professional Growth: Access to training, certifications, and development programs.
- Comprehensive Benefits:
- Competitive salary structure
- Annual leave and holiday benefits
- Health insurance for employees and dependents
- Retirement and savings plans
- TELUS Health Employee Assistance Programme – 24/7 well-being support
- Life assurance and income protection
- Additional perks like childcare vouchers, gym memberships, and flexible spending options
Inclusion and Diversity at ICON
ICON plc is an equal opportunity employer committed to building a diverse workforce and creating an inclusive environment. Applicants from all backgrounds are encouraged to apply, including those who may not meet every single requirement. ICON plc Hiring for Clinical Data Coordinator II
How to Apply?
Eligible and interested candidates can apply through the official ICON careers portal or trusted pharma job boards like PharmaBharat.com. Make sure your resume highlights your CDM experience, tools proficiency, and relevant project contributions. ICON plc Hiring for Clinical Data Coordinator II
[Apply Online at ICON Careers →] (Insert link if available)
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Final Thoughts
The Clinical Data Coordinator II role at ICON plc is a prime opportunity for life sciences professionals looking to make a tangible impact in global clinical research. With access to advanced tools, global trials, and industry best practices, this role prepares you for a long-term, successful career in data management and regulatory science. ICON plc Hiring for Clinical Data Coordinator II
Don’t miss this chance to join a world-class organization that is transforming the future of medicine through data.
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