ICON plc Announces Clinical Data Coordinator II Opening in Bangalore Under Hybrid Work Model

Global healthcare intelligence and clinical research organization ICON plc has invited applications for the position of Clinical Data Coordinator II (CDC II) within its Clinical Data Management (CDM) functional service provision division, ICON Strategic Solutions (FSP). The position is structured around a hybrid work setup operating out of ICON’s Bangalore office, catering to professionals seeking flexibility alongside rigorous clinical data oversight.

Position Summary & Strategic Focus

The CDC II role forms an integral part of ICON’s clinical operations, focusing on the delivery, validation, and maintenance of high-quality clinical trial datasets. Appointed candidates will collaborate directly with Data Management (DM) Trial Partners, clinical data scientists, and functional study leads to ensure end-to-end data integrity from study setup through closeout.

Primary Responsibilities

Clinical Data Review & Query Resolution: Systematically review diverse clinical datasets, listings, database formats, and analytics to maintain trial accuracy and completeness. Raise, track, and close electronic queries via EDC and CDMS platforms in direct collaboration with clinical site personnel.
Risk Management & Protocol Execution: Apply Data Management Monitoring (DMM) frameworks and Risk Assessment Categorisation Tools (RACT) across designated studies to mitigate procedural risks during data review cycles.
Data Reconciliation: Supervise and execute clinical and third-party data reconciliations adhering to specific data review plans, edit checks, and validation specifications.
Trial Deliverable Leadership: Proactively take ownership of independent data reviews under CDR oversight, maintain relevant trial master documentation, and ensure regulatory archival compliance.
Analytics & Audits: Leverage modern data visualization tools to support operational decision-making, assist in the maintenance of eCRFs and Study Specific Procedures (SSPs), and actively participate in regulatory audits and quality inspections.

Candidate Requirements

Educational Background: Bachelor’s degree in Life Sciences, Healthcare, Pharmacy, or a relevant scientific discipline.
Professional Experience: Intermediate-level hands-on exposure to clinical data management practices in a CRO, pharmaceutical, or biotechnology environment.
System Knowledge: Working familiarity with industry-standard EDC/CDMS tools such as Medidata Rave, Oracle RDC, or comparable applications.
Regulatory Understanding: Demonstrated comprehension of Good Clinical Practice (GCP) and ICH guidelines, alongside strong analytical problem-solving and communication skills.

Compensation & Organizational Perks

Flexible hybrid work arrangement
Comprehensive healthcare and medical insurance coverage for employees and families
Structured retirement savings and future financial planning schemes
Life assurance and wellness support via the 24/7 global LifeWorks Employee Assistance Programme
Local fringe benefits, including gym subsidies, child care support, and commuter assistance