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Senior Clinical Data Science Lead

Icon Plc
ICON PLC
8+ years
Not Disclosed
Bangalore, India
10 March 18, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Clinical Data Science Lead – Clinical Data Management & Analytics

Location: Bangalore, India
Job Type: Full-Time | Office with Flex
Company: ICON plc
Job ID: JR145679

About the Role
ICON plc, a global leader in healthcare intelligence and clinical research, is seeking a Senior Clinical Data Science Lead to drive data management and analytics strategy across clinical trials. This leadership role is critical in ensuring high-quality data delivery, effective study oversight, and successful execution of clinical development programs.

You will lead cross-functional teams, oversee end-to-end data management activities, and contribute to the advancement of innovative therapies through robust data science practices.

Key Responsibilities

  • Lead planning, development, and tracking of clinical data management deliverables including CRFs, data review plans, QC plans, and submission datasets

  • Ensure timely delivery of all study milestones and data outputs

  • Oversee database release planning, final dataset delivery, and archival processes

  • Act as the primary point of contact (POC) for assigned studies and clinical working groups

  • Collaborate with cross-functional teams to align data management strategies with study objectives

  • Identify and implement best practices, lessons learned, and process improvements

  • Ensure data quality, integrity, and compliance with regulatory standards

  • Manage vendor relationships and support global study execution

Required Qualifications & Experience

  • Bachelor’s degree in Life Sciences, Health Sciences, or a related field

  • Minimum 8+ years of experience in clinical data management or clinical data science

  • Proven experience as a lead or primary point of contact for clinical trials

  • Strong expertise in data management processes and complex trial oversight

  • Experience in project management and vendor management

  • In-depth understanding of clinical trial lifecycle and data workflows

  • Advanced proficiency in Microsoft Office and data analysis tools

  • Excellent organizational, communication, and leadership skills

  • Ability to work effectively in global, cross-functional environments

Preferred Skills

  • Experience in leading large-scale or complex global clinical trials

  • Exposure to regulatory submissions and data standardization practices

  • Strong analytical and strategic thinking capabilities

Why Join ICON
ICON offers a high-performance, collaborative environment where innovation and clinical research excellence drive impactful healthcare outcomes.

Key Benefits Include

  • Competitive salary and leadership career opportunities

  • Flexible work environment (office with flexibility)

  • Generous leave policies

  • Comprehensive health insurance

  • Retirement and financial planning benefits

  • Global Employee Assistance Programme (24/7 support)

  • Life insurance and wellness programs

  • Flexible, country-specific employee benefits

Diversity, Equity & Inclusion
ICON is committed to building an inclusive workplace. All qualified applicants will receive equal consideration without discrimination.

Application Note
Candidates who may not meet every requirement are encouraged to apply. ICON values diverse leadership experience and supports continuous professional growth.

This role is ideal for experienced clinical data leaders seeking to drive data science strategy, lead global trials, and contribute to advanced clinical development within a leading CRO.