ICON plc
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ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
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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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
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