PHARMAFull-time
Clinical Data Coordinator II (CDC II)
BANGALORE (IN)HYBRIDPOSTED: 9/23/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services

ROLE OVERVIEW
Deliver high-quality clinical data management tasks, maintaining eCRFs, data validation specifications, and supporting study metrics.
ROLE DEFINITION & RESPONSIBILITIES
- •Assist Data Management Study Lead in 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 status of study and task metrics to clinical data scientist, project team, and management
- •Address data related questions and recommend potential solutions
- •Identify root cause to systematically resolve data issues
Reporting Hierarchy: Reports to Data Management Study Lead • Sponsor-dedicated project team
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's degree in a relevant field such as Life Sciences or Healthcare
- Intermediate knowledge of clinical data management within pharmaceutical or biotech industry
- Familiarity with data management software and systems (e.g., Medidata, Oracle RDC)
- Strong attention to detail and ability to work in a fast-paced environment
PREFERRED QUALIFICATIONS
- •Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus
- •Excellent communication and cross-functional collaboration skills
REQUIRED VERIFIED SKILLS
Clinical Data Management
eCRF
Data Validation
Medical Data Reconciliation
Medidata
Oracle RDC
ICH-GCP
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Competitive base salary, health and wellbeing programs, retirement plans, learning and development opportunities
Competitive compensation package benchmarked against top clinical research organizations in India.
ORGANIZATION CONTEXT & CULTURE
ICON is the world’s largest FSP clinical research organisation supporting pharmaceutical and medical device partnerships globally.
TEAM SIZE: 10,000+ employees
INDUSTRY: Contract Research Organization (CRO) / Clinical Research / Healthcare Services
Culture: ICON fosters a collaborative and supportive global work environment focused on career development and employee wellbeing.
EXPECTED CAREER ROADMAP
Clear pathways for professional growth and advancement into senior data management roles within global FSP projects at ICON.
APPLICATION ADVISORY
Highlight your hands-on experience with clinical data management systems (like Medidata or Oracle RDC) and data reconciliation processes.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.
