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Senior Clinical Data Science Lead

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ICON
8+ years
₹28 LPA – ₹40 LPA (Estimated)
Bangalore, India
10 March 11, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Job Title: Senior Clinical Data Science Lead

Location: Bangalore, India (Office With Flexibility)

Company: ICON plc

Employment Type: Full-time

Salary: ₹28 LPA – ₹40 LPA (Estimated)


Job Description

ICON plc is seeking a Senior Clinical Data Science Lead to oversee clinical data management and analytics initiatives across clinical trials. In this leadership role, you will guide data science strategies, ensure data quality and compliance, and contribute to the successful execution of clinical studies.

You will work closely with cross-functional teams and clinical working groups to plan, manage, and deliver high-quality data management outputs that support regulatory submissions and clinical research outcomes.


Key Responsibilities

  • Lead the planning, tracking, and delivery of clinical data management deliverables, including CRFs, data review plans, QC plans, database release plans, and final datasets.

  • Ensure timely completion of all data management deliverables across assigned studies.

  • Serve as a key leader within clinical working groups, ensuring alignment between data management teams and therapeutic area trial requirements.

  • Oversee data quality, integrity, and compliance throughout the clinical trial lifecycle.

  • Identify and communicate lessons learned, best practices, and process improvements at the study level.

  • Support preparation of submission-ready datasets and archival documentation.

  • Collaborate with global teams to drive efficient data management strategies and trial execution.


Required Qualifications

  • Bachelor’s degree in Health Sciences, Life Sciences, or a related scientific discipline.

  • Minimum 8 years of experience leading clinical data management or clinical data science activities.

  • Experience serving as the main point of contact (POC) for clinical study data operations.

  • Strong background in clinical trial processes and study execution.

  • Proven experience working in global cross-functional teams.


Preferred Skills

  • Experience with clinical data management systems and processes.

  • Strong project management and vendor management capabilities.

  • Advanced proficiency with Microsoft Office tools for data analysis and reporting.

  • Excellent organizational, leadership, and communication skills.

  • Ability to manage multiple complex clinical studies simultaneously.


Benefits

Employees at ICON plc may receive benefits such as:

  • Competitive salary and performance incentives

  • Paid annual leave and holidays

  • Comprehensive health insurance coverage for employees and families

  • Retirement planning and savings programs

  • Global Employee Assistance Programme (TELUS Health) for mental health and wellbeing support

  • Life insurance coverage

  • Flexible benefits including childcare support, gym memberships, travel subsidies, and wellness programs


About the Company

ICON plc is a leading healthcare intelligence and clinical research organization partnering with pharmaceutical, biotechnology, and medical device companies to accelerate clinical development and bring innovative therapies to patients worldwide.