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Associate Director, Clinical Program Management

Takeda Pharmaceutical
10+ years
45 LPA - 70 LPA
Bangalore, India
1 June 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Associate Director, Clinical Program Management

Location: Bengaluru, India
Company: Takeda
Department: Clinical Operations / Clinical Development
Employment Type: Full-Time

Role Summary

The Associate Director, Clinical Program Management is responsible for leading operational strategy, planning, and execution of global clinical development programs. The role serves as a key Clinical Operations leader, ensuring studies are delivered on time, within budget, and in compliance with ICH-GCP, regulatory requirements, and Takeda SOPs.

This position collaborates closely with Clinical Operations Program Leads (COPLs), Clinical Study Managers (CSMs), CROs, investigators, and cross-functional stakeholders to translate Clinical Development Plans (CDPs) into executable operational strategies while driving clinical trial excellence across multiple regions.

Key Responsibilities

Clinical Program Strategy & Planning

  • Lead operational strategy development for assigned clinical programs.

  • Translate Clinical Development Plans (CDPs) into executable operational plans.

  • Evaluate multiple operational scenarios to optimize program execution.

  • Provide strategic inputs on:

    • Study Feasibility

    • Study Design

    • Timelines

    • Resource Planning

    • Budget Requirements

  • Ensure operational plans align with development objectives.

Clinical Study Execution Oversight

  • Oversee execution of global clinical studies.

  • Ensure studies are conducted according to:

    • ICH-GCP Guidelines

    • Local Regulatory Requirements

    • Takeda SOPs

  • Monitor study progress, milestones, risks, and deliverables.

  • Ensure studies are delivered:

    • On Time

    • Within Budget

    • With High Quality Standards

CRO & Vendor Management

  • Provide strategic oversight of:

    • CRO Partners

    • Functional Service Providers

    • External Vendors

  • Monitor vendor performance and compliance.

  • Ensure vendors meet contractual obligations and study deliverables.

  • Drive issue resolution and performance improvements.

Protocol & Clinical Development Support

  • Provide operational expertise for:

    • Protocol Synopsis Development

    • Protocol Design

    • Study Execution Planning

  • Gather operational feedback from investigators and sites.

  • Ensure protocol feasibility and patient/site burden considerations are addressed.

  • Support development of study execution strategies.

Budget & Financial Management

  • Lead clinical study budget planning and forecasting.

  • Monitor study expenditures and resource utilization.

  • Collaborate with:

    • Finance

    • Program Management

    • Procurement

    • CRO Partners

  • Ensure budget accuracy and cost control.

  • Manage external study spending and financial risks.

Site Selection & Feasibility

  • Participate in:

    • Site Selection

    • Investigator Selection

    • Feasibility Assessments

  • Provide regional and therapeutic expertise.

  • Ensure selected sites support study timelines and enrollment goals.

Risk Management & Monitoring

  • Review and approve:

    • Risk-Based Monitoring Plans

    • Monitoring Strategies

    • Study Risk Assessments

  • Track study-level:

    • Risks

    • Issues

    • Deviations

    • Corrective Actions

  • Support proactive risk mitigation and issue resolution.

Clinical Documentation Review

  • Provide operational review and input for:

    • Investigator Brochures (IBs)

    • Study Synopses

    • Protocols

    • Clinical Study Reports (CSRs)

    • Regulatory Submission Documents

  • Ensure operational feasibility and execution readiness.

Regulatory Inspection Readiness

  • Lead Clinical Operations inspection readiness activities.

  • Support:

    • Regulatory Inspections

    • Sponsor Audits

    • Quality Audits

  • Act as Clinical Operations SME during inspections.

  • Ensure compliance and audit preparedness.

Cross-Functional Leadership

  • Collaborate with:

    • Clinical Development

    • Medical Affairs

    • Regulatory Affairs

    • Biostatistics

    • Data Management

    • Quality Assurance

    • Pharmacovigilance

  • Drive alignment across global study teams.

  • Ensure successful program execution.

Business Development & Due Diligence

  • Support:

    • In-Licensing Activities

    • Business Development Evaluations

    • Alliance Assessments

  • Provide operational due diligence expertise.

  • Assess feasibility and operational risks of new opportunities.

Process Improvement & Innovation

  • Identify opportunities for:

    • Cost Reduction

    • Timeline Optimization

    • Quality Improvement

    • Operational Efficiency

  • Implement innovative ways of working across global clinical programs.

  • Promote operational excellence and continuous improvement.

People Development & Mentorship

  • Mentor and develop Clinical Operations professionals.

  • Share best practices and operational knowledge.

  • Support capability building within the Clinical Operations function.

  • Foster a culture of collaboration and excellence.

Required Qualifications

Education

One of the Following:

  • MBBS

  • MD

  • BDS

  • MDS

  • B.Pharm

  • M.Pharm

  • Pharm.D

  • B.Sc Life Sciences

  • M.Sc Life Sciences

  • Biotechnology

  • Biochemistry

  • Microbiology

  • Clinical Research

  • Nursing

  • Allied Health Sciences

Experience

  • 10+ years of Clinical Research and Clinical Operations experience.

  • Experience managing:

    • Global Clinical Trials

    • Clinical Development Programs

    • CRO Oversight

    • Clinical Study Execution

  • Experience in program-level clinical operations leadership.