Clinical Data Management Job at ICON
Looking for a Clinical Data Management Job with a global clinical research organisation? ICON Jobs offers an exciting opportunity for professionals passionate about clinical trials, data quality, and healthcare innovation. This hybrid CDC II role allows you to work on global clinical studies while collaborating with cross-functional teams. If you’re searching for Medical Jobs in India, this position offers excellent career growth in clinical data management and research.
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organisation dedicated to advancing innovative treatments and improving patient outcomes. With a strong presence across the globe, ICON partners with pharmaceutical, biotechnology, and medical device companies to deliver high-quality clinical development solutions. The company fosters an inclusive workplace that encourages innovation, collaboration, continuous learning, and professional growth while shaping the future of clinical research.
Job Details:
- Job Title: CDC II
- Job ID: JR150702
- Department: Clinical Data Management
- Division: ICON Strategic Solutions (FSP)
- Employment Type: Full-Time
- Work Arrangement: Hybrid
- Locations: Bengaluru, Chennai, Trivandrum
Job Description:
ICON is hiring a CDC II for its Clinical Data Management team under the ICON Strategic Solutions (FSP) division. This Clinical Data Management Job is ideal for professionals with experience in clinical trials, data review, and regulatory compliance. The selected candidate will be responsible for ensuring high-quality clinical data, collaborating with trial partners, supporting data review activities, and maintaining data integrity throughout the clinical trial lifecycle. Candidates exploring ICON Jobs and Medical Jobs in India will gain valuable experience in a global CRO environment.
Key Responsibilities:
- Plan, coordinate, and perform risk-based clinical data review activities.
- Define trial-specific data review requirements in collaboration with Trial Partners.
- Coordinate with programmers to establish data review tools.
- Monitor and communicate data review progress to Clinical Trial Data Managers (CTDM).
- Ensure timely completion of clinical data review deliverables.
- Support process and toolkit improvement initiatives.
- Drive risk-based data management approaches.
- Review clinical datasets, listings, reports, visualisations, and analytics for completeness and accuracy.
- Raise, manage, and resolve data queries using EDC/CDMS platforms.
- Develop Data Management Manuals (DMM) and review plans.
- Maintain clinical trial documentation and support data archival.
- Perform data reconciliation and quality checks.
- Contribute to dashboards and data visualisation activities.
- Support audits, inspections, and regulatory compliance.
- Assist with eCRF maintenance, validation specifications, and study procedures.
- Track study metrics and communicate project status.
- Investigate and resolve clinical data issues using root cause analysis.
Educational Requirements for this Clinical Data Management Job:
Candidates should possess:
- Bachelor’s degree in Healthcare or a related discipline.
Preferred Qualifications
- Experience in clinical data management within the pharmaceutical, biotechnology, or CRO industry.
- Familiarity with Medidata, Oracle RDC, or similar clinical data management systems.
- Knowledge of ICH-GCP guidelines and regulatory requirements.
Skills Required for this Clinical Data Management Job:
- Clinical Data Management
- Clinical Trial Data Review
- Clinical Research
- Data Validation
- Electronic Data Capture (EDC)
- eCRF Management
- Medidata
- Oracle RDC
- Data Reconciliation
- Data Integrity
- Risk Assessment
- Data Visualization
- Clinical Trial Documentation
- Regulatory Compliance
- ICH-GCP
- Analytical Thinking
- Attention to Detail
- Cross-functional Collaboration
- Communication Skills
- Problem-solving
