Life Sciences Job at ICON – Clinical Research Jobs | Clinical Data Coordinator II (CDC II)
Are you looking for a Life Sciences Job in the clinical research industry? ICON Careers is hiring for the Clinical Data Coordinator II (CDC II) role in Bangalore, Chennai, Trivandrum, and Bengaluru. This opportunity is ideal for Life Sciences and Healthcare graduates aiming to build long-term careers in Clinical Research Jobs and Clinical Data Management with a leading clinical research organisation.
About ICON plc
ICON plc is a healthcare intelligence and clinical research organisation dedicated to advancing innovative treatments and improving patient outcomes worldwide. The company promotes an inclusive work environment that supports collaboration and excellence. Through its expertise in clinical development, ICON provides professionals with opportunities to contribute to global clinical research programs while advancing their careers in healthcare and data management.
Job Details
| Company | ICON plc |
| Job Title | Clinical Data Coordinator II (CDC II) |
| Department | ICON Strategic Solutions (FSP) |
| Location | Bangalore, Chennai, Trivandrum, and Bengaluru (Remote or Office options) |
| Qualification | Bachelor’s degree in Life Sciences or Healthcare |
Job Description
The Clinical Data Coordinator II (CDC II) role at ICON involves supporting clinical data management activities within ongoing clinical development programs. Professionals in this Life Sciences Job will work closely with the Data Management Study Lead to maintain electronic Case Report Forms (eCRFs), Data Validation Specifications, and study-specific procedures. The role also includes reconciliation of clinical and third-party data, ensuring compliance with established edit specifications and data review plans in alignment with ICH-GCP standards.
This position contributes directly to data integrity and regulatory compliance in clinical trials, supporting cross-functional teams and ensuring that high-quality clinical data is delivered for analysis and reporting.
Key Responsibilities
- Assist the Data Management Study Lead in the maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.
- Manage clinical and third-party data reconciliation based on edit specifications and data review plans.
- Track and communicate the status of study and task metrics to the clinical data scientist, project team, and functional management.
- Address data-related questions and recommend potential solutions.
- Identify root causes to systematically resolve data issues.
- Deliver clinical data management work to a high standard while collaborating with team members and stakeholders.
Eligibility Criteria
- Education: Bachelor’s degree in a relevant field such as Life Sciences or Healthcare.
- Experience: Intermediate knowledge of Clinical Data Management within the pharmaceutical or biotechnology industry.
Required Skills
- Familiarity with data management software such as Medidata, Oracle RDC, or similar systems.
- Knowledge of regulatory guidelines and standards (ICH-GCP) is an added advantage.
- Strong attention to detail.
- Excellent communication skills.
- Ability to collaborate with cross-functional teams.
- Analytical and problem-solving abilities.
- Clinical data management and data reconciliation expertise.
- Ability to work effectively in a professional environment.
Benefits
ICON offers a competitive salary along with comprehensive employee benefits, including:
- Various annual leave entitlements.
- Health insurance offerings for employees and their families.
- Competitive retirement planning options.
- Global Employee Assistance Programme (LifeWorks).
- Life assurance.
- Flexible country-specific benefits such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, and health assessments.
How to Apply
Apply online through the official ICON Careers page using the link below.
Why Join ICON Careers for Clinical Research Jobs?
This Life Sciences Job offers exposure to structured clinical development programs and clinical data management practices aligned with international standards. Working as a Clinical Data Coordinator II enables professionals to strengthen their expertise in data reconciliation, regulatory compliance, and cross-functional collaboration. For candidates exploring Clinical Research Jobs at a recognised clinical research organisation, this role provides a platform to build specialised experience in Clinical Data Management.
If you are seeking a Life Sciences Job with ICON Careers, this Clinical Data Coordinator II opportunity is a suitable step toward advancing your profile in Clinical Research Jobs and Clinical Data Management. Review the eligibility criteria and apply through the official link provided above.
