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Associate Director, Gcp Compliance

Takeda Pharmaceutical
Takeda Pharmaceutical
8+ years
$153,600 – $241,340
10 Jan. 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Job Title: Associate Director – GCP Compliance

Location: Remote / Massachusetts, USA
Department: Clinical Development / Quality & Compliance
Employment Type: Full-Time, Remote

Role Overview:
Takeda is seeking an experienced Associate Director, GCP Compliance to lead and oversee Good Clinical Practice (GCP) compliance across clinical trial delivery functions. This senior role is responsible for ensuring high-quality standards in clinical trials through risk-based assessments, compliance management, internal audits, and KPI-driven reporting. The position requires strategic leadership, cross-functional collaboration, and global perspective to maintain Takeda’s commitment to integrity, innovation, and patient-focused research.

Key Responsibilities:

  • Lead the implementation of GCP compliance management across clinical trial delivery functions.

  • Oversee quality events, deviations, root cause analysis, CAPA development, and effectiveness checks.

  • Facilitate internal audits, prepare study teams, manage audit responses, and ensure corrective and preventive actions (CAPA) are completed.

  • Conduct proactive risk-based compliance assessments for clinical functions and advise on mitigation strategies.

  • Develop, track, and report GCP compliance metrics and KPIs to leadership, including trends, risks, and performance analytics.

  • Collaborate with cross-functional teams, R&D QA, and external partners to ensure adherence to Takeda SOPs, ICH-GCP, and regulatory requirements.

  • Mentor, coach, and develop team members, fostering a culture of compliance, innovation, and professional growth.

Qualifications & Experience:

  • Bachelor’s degree in Life Sciences or related field; advanced degree preferred.

  • 8+ years of experience in the pharmaceutical or clinical research industry, with at least 6 years in compliance, GCP, or clinical study management.

  • Proven experience leading projects, managing cross-functional teams, and implementing clinical compliance strategies.

  • Global/international experience, with ability to collaborate across regions.

  • Strong knowledge of clinical development processes, operational excellence, and regulatory standards.

  • Excellent strategic thinking, planning, communication, and problem-solving skills.

  • Demonstrated ability to implement novel approaches and drive operational improvements in clinical compliance.

Why Join Takeda:

  • Lead compliance and quality excellence in global clinical development programs.

  • Remote work flexibility while contributing to impactful, patient-focused clinical trials.

  • Competitive base salary: $153,600 – $241,340 plus potential incentives.

  • Comprehensive benefits including healthcare, 401(k) matching, paid time off, tuition reimbursement, and wellness programs.

  • Join a values-led, inclusive, and innovative organization recognized globally as a Top Employer.

Equal Opportunity Statement:
Takeda is committed to diversity, equity, and inclusion. Employment decisions are made without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics.