Hybrid Clinical Research Job at ICON plc
Hybrid Clinical Research Job at ICON plc
Looking for a Hybrid Clinical Research Job with a globally recognized clinical research organization? ICON plc Careers has announced an exciting opportunity for the position of Clinical Data Coordinator II across Bangalore, Chennai, and Trivandrum with flexible remote or office work options. If you have a Life Sciences background and experience in clinical data management, this is an excellent opportunity to build your career in one of the world’s leading healthcare intelligence organizations. Explore this latest opening and take the next step toward rewarding Life Science Jobs with global exposure.
About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization that partners with pharmaceutical, biotechnology, and medical device companies to accelerate clinical development. Through cutting-edge technology, scientific expertise, and global clinical operations, ICON supports the development of innovative medicines that improve patient outcomes worldwide. ICON plc Careers offer professionals exciting opportunities across clinical operations, data management, regulatory affairs, biostatistics, and healthcare research. With an employee-focused culture, flexible work options, and continuous learning opportunities, ICON remains one of the top employers for professionals seeking Life Science Jobs.
Job Details:
- Job Title: Clinical Data Coordinator II
- Company: ICON Strategic Solutions (FSP)
- Department: Clinical Data Management
- Locations: Bengaluru, Bangalore, Chennai, and Thiruvananthapuram (Remote or Office)
Role Overview
ICON Strategic Solutions is seeking a Clinical Data Coordinator II to support clinical data management activities for clinical research studies. The role involves maintaining electronic Case Report Forms (eCRFs), performing clinical and third-party data reconciliation, ensuring data quality, resolving data discrepancies, and collaborating with cross-functional teams to support the successful execution of clinical trials. The position contributes to the delivery of high-quality clinical data that supports regulatory submissions and the development of innovative therapies.
Key Responsibilities
- Assist the Data Management Study Lead in maintaining electronic Case Report Forms (eCRFs), Data Validation Specifications (DVS), and Study-Specific Procedures.
- Perform clinical and third-party data reconciliation in accordance with edit specifications and data review plans.
- Track study progress and communicate the status of study activities and task metrics to Clinical Data Scientists, project teams, and functional management.
- Respond to data-related queries and recommend appropriate solutions to ensure data quality and integrity.
- Identify root causes of data discrepancies and implement systematic corrective actions.
- Review, clean, and validate clinical trial data to ensure completeness, consistency, and compliance with study requirements.
- Collaborate with cross-functional teams to support timely database cleaning, data review, and study deliverables.
- Maintain compliance with applicable regulatory requirements, Good Clinical Practice (GCP), and organizational Standard Operating Procedures (SOPs).
Required Qualifications
- Bachelor’s degree in Life Sciences, or a related discipline.
Required Experience
- Relevant experience in Clinical Data Management within the pharmaceutical, biotechnology, or clinical research industry.
- Working knowledge of clinical data management processes and clinical trial data workflows.
- Experience using clinical data management systems such as:
- Medidata Rave
- Oracle RDC
- Similar Electronic Data Capture (EDC) platforms
Preferred Knowledge
- Understanding of ICH-GCP guidelines and clinical research regulations.
- Familiarity with clinical trial documentation, data validation, and reconciliation processes.
Technical Skills
- Electronic Data Capture (EDC) systems
- eCRF design and maintenance
- Data Validation Specifications (DVS)
- Clinical data reconciliation
- Clinical database review and cleaning
- Clinical data quality management
- Root cause analysis and issue resolution
- Clinical trial documentation
Key Competencies
- Strong analytical skills and attention to detail.
- Excellent problem-solving and data interpretation abilities.
- Effective written and verbal communication skills.
- Ability to collaborate with multidisciplinary and cross-functional teams.
- Strong organizational and time management skills.
- Ability to work efficiently in a fast-paced clinical research environment.
Work Arrangement
- Location: Bengaluru, Chennai, or Thiruvananthapuram, India
- Work Model: Remote or Office
