Senior Clinical Data Coordinator

ICON plc

. Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements .

Posted 9/18/2026full-timeBangalore • IndiaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical data management, ensuring compliance with regulatory standards while collaborating effectively with cross-functional teams. Proficient in data management strategies and mentoring junior staff to enhance data quality and streamline processes.

Highest-signal resume keywords

Clinical Data ManagementData Management SoftwareRegulatory Guidelines KnowledgeAttention To DetailCommunication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ReconciliationData CodingData CleaningData Quality EnhancementStudy Documentation Management

Soft Skills

CollaborationMentoringProblem SolvingAdaptability

Tools & Technologies

MedidataOracle RDC

Industry Keywords

Pharmaceutical IndustryBiotechnology IndustryICH-GCPStudy Lifecycle

Tech Stack

Tools & technologies

Oracle

About the role

Key responsibilities & impact

Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements
Identify and resolve data discrepancies and issues to streamline data flow and enhance data quality throughout the study lifecycle
Collaborate with clinical operations and biostatistics teams to develop and execute study-specific data management strategies
Perform project activities such as filing and archiving study documentation and dispatching queries to investigator sites
Mentor junior data coordinators on data reconciliation, coding, and cleaning procedures
Lead clinical research tasks requiring technical depth, with a focus on quality and continuous improvement
Ensure study timelines are met

Requirements

What you’ll need

Bachelor's degree in a relevant field, such as Life Sciences or Healthcare
Proven experience in clinical data management within the pharmaceutical or biotechnology industry
Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar)
Strong attention to detail and the ability to work effectively in a fast-paced environment
Excellent communication skills and the ability to collaborate with cross-functional teams
Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus
Willingness to travel as required (approximately 5%)
Legal right to work in the country where the role is based

Benefits

Comp & perks

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways