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Executive Director, Clinical Operations

12-15 years
$205,100 – $322,300 (USD)
10 April 29, 2025
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: Executive Director, Clinical Operations

  • Company: Takeda

  • Location: Boston, Massachusetts

  • Job ID: R0147752

  • Date Posted: March 24, 2025

  • Job Level: Senior

  • Job Type: Full Time

  • Worker Type: Employee

  • Worker Sub-Type: Regular

  • Travel Requirement: Minimal (up to 25%)

  • Work Arrangement: Hybrid

  • Industry: Pharmaceutical / Clinical Research

  • Department: Global Clinical Development Operations

  • Reports To: Head of Global Clinical Development Operations

  • Salary Range: $205,100 – $322,300 (USD)

  • Bonus/Incentives: Eligible for short-term and/or long-term incentives

  • Benefits:

    • Medical, dental, vision insurance

    • 401(k) with match

    • Disability coverage

    • Basic life insurance

    • Tuition reimbursement

    • Paid vacation (up to 120 hours/year)

    • Sick time (up to 80 hours/year)

    • Paid volunteer time off

    • Company holidays

    • Wellness programs


Role Summary

Lead global clinical operations within assigned therapeutic areas with direct and indirect team management. Own strategic execution of global clinical trials (Phases I–IV), financial oversight, vendor governance, and regulatory compliance, especially in oncology.


Key Responsibilities

  • Lead operational strategy and execution of global clinical trials

  • Represent GCDO in TA forums and review boards

  • Manage global clinical operations teams (directly and in matrix settings)

  • Drive compliance, process improvement, and risk mitigation initiatives

  • Oversee study budgets and forecasts across therapeutic units

  • Maintain vendor relationships and CRO partnerships

  • Approve due diligence for new assets and alliances


Required Qualifications

  • Bachelor’s degree in Life Sciences (advanced degree preferred)

  • 15+ years in pharma/clinical research (12+ in clinical program management, 6+ in line management)

  • Deep oncology experience through Phases I–IV

  • Expert knowledge of FDA, EUCTR, ICH-GCP, and global clinical research regulations

  • Global leadership and cross-cultural team management experience


Competencies

  • Strategic leadership and organizational transformation

  • Financial acumen in budget planning and oversight

  • High-level stakeholder collaboration

  • Operational excellence and innovation mindset


EEO Statement

Takeda is an equal opportunity employer, committed to diversity and inclusion across all levels.