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 role is

not suitable for freshers .

Senior‑level clinical development and therapeutic leadership experience is essential.

Pharma, life sciences, or healthcare qualification relevant to the role.