ICON plc

Senior Director, Therapeutic Area

ICON plc$150K — $200K *
US-AnywhereRemote in Blue Bell, PA
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Deep expertise in oncology drug development, specifically in solid tumors and/or hematologic malignancies.
  • Strong understanding of oncology clinical trial design and evolving treatment landscapes.
  • Proven ability to engage with senior stakeholders in a strategic, client-facing manner.
  • Excellent communication and presentation skills for translating complex data into actionable insights.
  • Collaborative mindset with cross-functional teamwork abilities in a global context.
  • MD or PhD required.

Responsibilities

  • Lead strategic oncology drug development program design, delivering tailored solutions.
  • Own protocol development for oncology clinical trials, including design and evaluation.
  • Partner with senior client stakeholders to provide expert guidance on oncology strategies.
  • Act as the scientific and strategic lead in proposal development and bid defense activities.
  • Build relationships with oncology key opinion leaders and regulatory bodies.
  • Contribute to new oncology-focused service offerings to support area growth.
  • Provide training, mentorship, and thought leadership in oncology to teams and clients.

Benefits

  • Health and wellbeing programs including medical, dental, and vision coverage as applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programs and wellbeing resources.
  • Opportunities for learning and development through structured training.
Full Job Description
Sr Director Therapeutic Area (Oncology)- Blue Bell, PA- Remote

Senior Director, Drug Development & Consulting - Oncology

At ICON plc, we are driven by a commitment to People, Clients, and Performance. We are seeking a strategic Oncology expert to join our Drug Development & Consulting team in a highly visible, client-facing role.

This position offers the opportunity to act as a trusted advisor to senior stakeholders across the industry, including CEOs, CMOs, and Oncology Therapeutic Area Heads. You will deliver bespoke, asset-centric solutions while shaping oncology drug development strategies across the full lifecycle.

The Role

This is a consultative and advisory role where you will serve as a key scientific partner to both external clients and internal teams. Often acting as the first technical point of contact, you will play a critical role in pre-sales activities, proposal strategy, and long-term partnership development within oncology.

Key Responsibilities
  • Lead strategic oncology drug development program design, delivering tailored, asset-focused solutions across solid tumors and/or hematologic malignancies
  • Own protocol development, including design, review, and evaluation for oncology clinical trials
  • Partner directly with senior client stakeholders to provide expert guidance on oncology data interpretation and development strategy
  • Act as the scientific and strategic lead in proposal development and bid defense activities
  • Build and maintain relationships with oncology key opinion leaders, advisory boards, and regulatory bodies
  • Contribute to the development of new oncology-focused service offerings and support growth in this therapeutic area
  • Provide training, mentorship, and thought leadership in oncology to internal teams and external clients
  • Participate in portfolio reviews, governance activities, and project oversight as needed
  • Support operational teams with scientific input, including investigator meetings and oncology-specific project discussions
  • Represent ICON at oncology congresses and scientific meetings to promote clinical and scientific excellence

What You Bring
  • Deep expertise in oncology drug development (solid tumors and/or hematologic malignancies)
  • Strong understanding of oncology clinical trial design, endpoints, and evolving treatment landscapes (e.g., immuno-oncology, targeted therapies)
  • Proven ability to operate in a strategic, client-facing, and consultative environment
  • Experience engaging with senior stakeholders and influencing decision-making
  • Excellent communication and presentation skills, with the ability to translate complex oncology data into actionable insights
  • A collaborative mindset with the ability to work cross-functionally in a global environment
  • MD or PhD required.


Additional Information
  • Approximately 30-40% travel (domestic and international)
  • Opportunity to work in a highly visible, impact-driven role shaping the future of oncology drug development


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Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways


Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Are you a current ICON Employee? Please click here to apply

About ICON plc

ICON plc is a global provider of drug development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development. ICON has approximately 15700 employees in 40 countries. The company was founded in Dublin, Ireland in 1990 and is headquartered in Leopardstown, Dublin. ICON has been publicly traded on the NASDAQ since 1998.
Learn more about ICON plc
Size
39,300 employees
Market Cap
$16.2 billion
Industry
Net Income
$332.3 million
Founded
2017
5 Year Trend
+26.9%
Revenue
$2.7 billion
NASDAQ

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