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Senior Clinical Data Science Lead

0-2 years
Not Disclosed
10 April 17, 2025
Job Description
Job Type: Full Time Remote 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: Taipei
Job ID: 2025-117611
Department: Clinical Data Management, Clinical Systems, Data Standards Consultant
Division: ICON Strategic Solutions
Work Type: Remote
Company: ICON plc
Hiring Manager: Huixin "Stella" Song
Actions: Apply | Shortlist | Send a Message to Hiring Manager


About the Role

As a Senior Clinical Data Science Lead, you will join the world’s largest and most comprehensive clinical research organization, empowered by healthcare intelligence. You will be a key leader in managing clinical data across global trials and ensuring delivery excellence in data management.


Key Responsibilities

  • Serve as an escalation point for data issues with CROs, vendors, and internal stakeholders

  • Track data quality and submission readiness of CRF and non-CRF deliverables, including CDISC data packages

  • Lead project management of all data management deliverables, ensuring timelines, costs, and quality

  • Implement clinical data collection strategies aligned with global business and CDISC standards

  • Oversee CROs executing Phase I–IV trials, representing Data Management on Global Trial Teams

  • Drive operational planning for all DM-related trial documents (e.g., Data Management Plan)

  • Manage clinical data-related CAPAs and partner in audit responses and quality assurance

  • Contribute to clinical trial budgeting, forecast, and operational efficiency

  • Provide input on protocol design, integrated analysis plans, and CSR development

  • Support SOP development and continuous improvement initiatives within the department


Qualifications and Requirements

  • Advanced degree in Life Sciences, Mathematics, Computer Science, or equivalent experience

  • Therapeutic area expertise in Oncology and/or Neurology

  • Strong background in clinical development and cross-functional collaboration

  • Proficiency with EDC systems such as InForm™, Rave, and additional tools (ePRO, eHR, etc.)

  • Knowledge of ICH-GCP, CDISC standards, and global health authority regulations (FDA, EMA, PMDA, etc.)

  • Understanding of coding systems, SAE reconciliation, and clinical data terminologies

  • Strong computer skills (MS Office) and familiarity with SAS, SQL, or similar programming languages


What ICON Offers

ICON provides a globally competitive compensation package and a culture built on performance, growth, and flexibility.

Benefits Include:

  • Annual leave entitlements tailored by location

  • Customizable health insurance for individuals and families

  • Competitive retirement planning

  • Global Employee Assistance Programme (TELUS Health) – 24/7 access to support

  • Life assurance

  • Optional benefits such as:

    • Childcare vouchers

    • Bike-to-work schemes

    • Discounted gym memberships

    • Health assessments

    • Subsidized transport options

Full details available at: ICON Benefits Overview


Inclusion & Accessibility

ICON is committed to an inclusive, diverse, and accessible workplace. Reasonable accommodations for applicants with disabilities are available throughout the recruitment process.
Learn more:
ICON Accommodations Policy


Encouragement to Apply

Not sure if you meet all the criteria? ICON encourages you to apply anyway—you might be the perfect fit for this or other open positions.