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Associate Director, Clinical Program Management

Takeda Pharmaceutical
10+ years
INR ₹35 – ₹50 LPA
Bangalore, Karnataka, India
10 June 16, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, 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

Role Purpose

Lead operational strategy, planning, and execution of global clinical studies within assigned clinical development programs. The role ensures studies are delivered according to quality, timelines, and budget requirements while supporting the overall Clinical Development Plan (CDP).

Working closely with the Clinical Operations Program Lead (COPL), Clinical Study Managers (CSMs), CROs, investigators, and cross-functional stakeholders, the incumbent serves as a strategic clinical operations leader for global development programs.


Key Responsibilities

1. Clinical Program Strategy & Planning

  • Develop regional operational strategies for assigned clinical programs.

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

  • Evaluate multiple operational scenarios to optimize study execution.

  • Provide strategic input on:

    • Feasibility

    • Timelines

    • Budgets

    • Site strategy

    • Country selection

  • Support protocol development and study design discussions.


2. Clinical Study Oversight

  • Oversee execution of Phase I, II, and III clinical studies.

  • Ensure compliance with:

    • ICH-GCP

    • Local regulations

    • Takeda SOPs

    • Global quality standards

  • Monitor study progress against key milestones.

  • Ensure delivery on schedule and within budget.


3. CRO & Vendor Management

  • Provide oversight of strategic CRO partners and vendors.

  • Monitor:

    • Performance

    • Deliverables

    • Timelines

    • Quality metrics

    • Budget utilization

  • Ensure vendor compliance with regulatory and company requirements.


4. Budget & Financial Management

  • Lead study budget planning and forecasting.

  • Manage external study expenditures.

  • Collaborate with:

    • Finance

    • Program Management

    • Outsourcing Teams

    • CRO Partners

  • Review and validate budget assumptions and spending.


5. Risk Management & Quality Oversight

  • Review Risk-Based Monitoring (RBM) strategies.

  • Approve monitoring plans and quality documents.

  • Identify:

    • Study risks

    • Site trends

    • Operational challenges

  • Develop mitigation and contingency plans.


6. Clinical Documentation Review

Provide operational review and input for:

  • Protocols

  • Protocol Synopses

  • Investigator Brochures

  • Clinical Study Reports

  • Regulatory Meeting Packages

  • Trial Execution Plans


7. Inspection Readiness & Regulatory Support

  • Lead Clinical Operations inspection readiness activities.

  • Support:

    • Regulatory inspections

    • Audits

    • Health authority interactions

  • Serve as Clinical Operations Subject Matter Expert (SME).


8. Cross-Functional Leadership

  • Collaborate across:

    • Clinical Development

    • Medical Affairs

    • Regulatory Affairs

    • Biostatistics

    • Data Management

    • Safety

    • External Partners

  • Represent Clinical Operations in global governance discussions.


9. Business Development Support

  • Participate in:

    • Due diligence activities

    • In-licensing evaluations

    • Alliance assessments

  • Provide operational feasibility assessments for new opportunities.


10. Talent Development & Mentoring

  • Coach and mentor junior Clinical Operations professionals.

  • Share knowledge and best practices.

  • Support capability-building initiatives across the organization.


Required Qualifications

Education

Required

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Related Scientific Discipline

Preferred

  • Advanced Degree (Master's, PharmD, PhD, MBA)


Experience Requirements

Total Experience

  • 10+ years in:

    • Pharmaceutical Industry

    • Biotechnology Industry

    • Clinical Research Organizations (CROs)

Clinical Study Management Experience

  • 7+ years of clinical study management and oversight experience.

Mandatory Experience

  • Global Clinical Trials

  • Multi-country Studies

  • Phase I Studies

  • Phase II Studies

  • Phase III Studies

  • Multiple Therapeutic Areas

  • CRO Oversight

  • Budget Management

  • Inspection Readiness


Core Competencies

Clinical Operations Expertise

  • Clinical Development Planning

  • Study Execution

  • Global Trial Management

  • Risk Management

  • Operational Feasibility


Leadership Skills

  • Cross-functional leadership

  • Stakeholder management

  • Team development

  • Influencing skills

  • Strategic thinking


Communication Skills

  • Excellent written communication

  • Executive presentations

  • Conflict resolution

  • Negotiation and collaboration


Problem Solving

  • Scenario planning

  • Risk assessment

  • Contingency planning

  • Process improvement


Travel Requirements

  • Approximately 5–20% travel

  • Domestic and international travel

  • CRO, investigator, and Takeda site visits


Likely Job Level

Based on the responsibilities, experience, global scope, and leadership expectations, this role aligns with:

  • Associate Director, Clinical Operations

  • Senior Manager, Clinical Operations

  • Clinical Operations Program Lead

  • Global Study Management Lead

  • Clinical Trial Program Lead