Senior Director, Therapeutic Area

Senior Director, Therapeutic Area (Oncology/Hematology)

Company: ICON plc
Job Title: Senior Director, Therapeutic Area – Oncology/Hematology
Locations:

• Blue Bell, Pennsylvania, USA (Remote)
• Mechelen, Belgium
• Reading, United Kingdom

Job Type: Full-Time
Work Mode: Remote / Hybrid
Industry: Clinical Research / Oncology / Pharmaceutical / CRO
Experience Required: 12–18+ Years
Travel Requirement: Approximately 30% Global Travel

Job Overview

ICON plc is seeking an experienced and strategic Senior Director, Therapeutic Area (Oncology/Hematology) to lead global oncology and hematology clinical development initiatives. This leadership role focuses on driving therapeutic area strategy, overseeing complex clinical programs, and ensuring operational excellence across international clinical research projects.

The selected candidate will work closely with internal leadership teams, sponsors, clinical operations, and regulatory stakeholders to advance innovative oncology therapies and improve global patient outcomes.

This opportunity is ideal for senior clinical development professionals with deep expertise in oncology, hematology, clinical trials, therapeutic strategy, and pharmaceutical leadership.

Key Responsibilities

Therapeutic Area Leadership

• Lead strategic direction and operational execution for the Oncology/Hematology therapeutic area.
• Develop and implement long‑term therapeutic strategies aligned with organizational goals.
• Drive innovation and scientific excellence across oncology clinical development programs.
• Provide leadership guidance for global clinical research initiatives and cross‑functional teams.

Clinical Development & Trial Oversight

• Oversee the design, planning, and execution of:
  • Oncology clinical trials
  • Hematology studies
  • Global development programs
• Ensure studies meet:
  • Regulatory requirements
  • Scientific standards
  • Ethical guidelines
  • Sponsor expectations
• Support successful delivery of clinical programs from early development through late-stage trials.

Strategic Collaboration & Stakeholder Management

• Collaborate with:
  • Clinical operations teams
  • Regulatory affairs
  • Medical affairs
  • Sponsors
  • Global stakeholders
• Build strong partnerships to enhance program outcomes and operational performance.
• Address clinical and operational challenges while ensuring alignment across teams.

Regulatory Compliance & Industry Excellence

• Ensure compliance with:
  • Global regulatory requirements
  • ICH‑GCP guidelines
  • Clinical research standards
  • Internal quality policies
• Implement industry best practices in therapeutic area management.
• Support audit readiness and regulatory inspection preparedness.

Scientific Innovation & Industry Awareness

• Stay informed about:
  • Oncology research advancements
  • Hematology treatment innovations
  • Emerging therapeutic trends
  • Competitive clinical landscapes
• Drive continuous improvement and maintain a competitive edge in clinical development strategy.

Required Qualifications

Educational Qualification

Mandatory:

• MD (Doctor of Medicine) OR
• PhD in a relevant scientific or medical discipline

Preferred Background

• Oncology
• Hematology
• Clinical Research
• Pharmaceutical Sciences
• Translational Medicine
• Drug Development

Experience Requirements

Mandatory Experience

• Extensive experience in:
  • Clinical development
  • Therapeutic area leadership
  • Oncology or hematology clinical research
  • Strategic clinical operations
• Proven track record of:
  • Leadership success
  • Global clinical program management
  • Cross-functional collaboration
  • Operational execution

Preferred Experience

• Experience managing:
  • International oncology studies
  • Global clinical teams
  • Multidisciplinary research programs
• Strong exposure to:
  • Regulatory interactions
  • Sponsor management
  • CRO environments
  • Pharmaceutical development strategy

Estimated Experience Level

• Typically suited for professionals with 12–18+ years of relevant industry experience.

Freshers Eligibility

• This