PHARMAFull-time
Clinical Data Coordinator - Senior
BANGALORE (IN)HYBRIDPOSTED: 9/19/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ROLE OVERVIEW
Senior Clinical Data Coordinator supporting sponsor-dedicated clinical research programmes through clinical data management planning, discrepancy resolution, cross-functional collaboration, study documentation, data reconciliation, coding, cleaning, and mentoring of junior coordinators.
ROLE DEFINITION & RESPONSIBILITIES
- •Create and maintain detailed clinical data management plans and documentation
- •Identify and resolve data discrepancies and issues to improve data quality and data flow
- •Collaborate with clinical operations and biostatistics teams on study-specific data management strategies
- •Support project activities including documentation filing, archiving, and dispatching queries to investigator sites
- •Mentor junior data coordinators on data reconciliation, coding, and cleaning
- •Contribute to quality improvement and timely study delivery
- •Perform additional project activities required to meet study timelines
Reporting Hierarchy: Works within ICON Strategic Solutions' sponsor-dedicated model and collaborates with clinical operations, biostatistics, investigator sites, and other cross-functional study teams; Specific reporting manager is not stated
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's degree in a relevant field such as Life Sciences or Healthcare
- Proven clinical data management experience within the pharmaceutical or biotechnology industry
- Familiarity with clinical data management software and systems
- Strong attention to detail
- Ability to work independently in a fast-paced environment
- Excellent communication and cross-functional collaboration skills
PREFERRED QUALIFICATIONS
- •Knowledge of ICH-GCP and regulatory guidelines
- •Experience with Medidata or Oracle RDC
- •Experience mentoring junior data coordinators
- •Clinical data reconciliation, coding, and cleaning experience
- •Willingness to travel approximately 5%
REQUIRED VERIFIED SKILLS
Clinical Data Management
Data Management Plans
Clinical Data Review
Data Discrepancy Resolution
Data Reconciliation
Clinical Data Coding
Data Cleaning
Medidata
Oracle RDC
ICH-GCP
Clinical Research Documentation
Regulatory Compliance
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Bonus & Equity: Performance related incentives
Benefits: Competitive base salary and performance-related incentives; health and wellbeing programmes including applicable medical, dental and vision coverage; retirement and pension plans; life assurance and disability coverage; employee assistance programmes; learning and development opportunities
The posting states a competitive base salary and performance-related incentives but does not disclose salary figures. No numerical compensation has been inferred.
ORGANIZATION CONTEXT & CULTURE
ICON is a global clinical research organisation providing outsourced development and commercialisation services to pharmaceutical, biotechnology, and healthcare organisations. ICON Strategic Solutions provides sponsor-dedicated clinical research support.
TEAM SIZE: 40,000+ employees
INDUSTRY: Contract Research Organization (CRO) / Clinical Research / Healthcare Services
Culture: ICON describes a collaborative, sponsor-dedicated environment focused on quality, career development, inclusion, accessibility, and advancing treatments for patients worldwide.
EXPECTED CAREER ROADMAP
Senior Clinical Data Coordinator experience can progress toward Data Management Lead, Clinical Data Management Lead, Project Data Management, or broader clinical research data leadership roles, depending on expertise and organisational opportunities.
APPLICATION ADVISORY
Emphasize senior-level clinical data management experience, study lifecycle knowledge, data management plans, discrepancy resolution, reconciliation, coding and cleaning; highlight Medidata or Oracle RDC experience; demonstrate cross-functional collaboration and mentoring; mention ICH-GCP knowledge and measurable quality or timeline improvements.
RECOMMENDED TRAINING
1/5
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