Associate Director Informaticist
ICON plc
Summary
The purpose of the Associate Director Informaticist role is to support the design of clinical programs and trials by bringing together internal and external data (e.g., prevalence data, real world data and analytics, electronic Clinical Outcome Assessments, and Schedule of Activities) analyses and insights to develop and inform asset profile, program strategy, and trial designs, while driving excellence and optimization, enabling more efficient planning and execution.
Job description
What You Will Do
- Responsible for leading the approach to program design, placement decisions, and related considerations (e.g., scaling of Decentralized Clinical Trials, Value Based Research principles, and enabling goals for diverse representation in clinical trials, etc.)
- Responsible for developing and leading the approach to data taxonomies in support of eCOA and SoA designs and related considerations
- Responsible for driving standardization in design within and across therapeutic areas via utilization of taxonomies
- Responsible for communicating insights for strategies that can optimize trial and program design for time, value, cost, and/or risk considerations while creating accessibility and pathways for participation in clinical trials
- Collaborate with asset team to bring data and insights to support asset strategy, program, and trial design decisions
- Anticipate and ensure completion of modeling and scenario needs by applying clinical development, TA, and analytics expertise
- Support the use of real-world data and collaborate cross functionally to bring to inform design
- Promote data-driven and risk-based decision making
Your Profile
Required qualifications and experience:
- Bachelor's Degree in a scientific or health-related field Minimum 5 years' experience in the pharmaceutical industry, drug development, and/or related fields
- Therapeutic expertise and knowledge of the clinical research landscape; ability to acquire and maintain expertise to support portfolio needs
Requirements
- Bachelor's Degree in a scientific or health-related field
- Minimum 5 years' experience in the pharmaceutical industry, drug development, and/or related fields
- Therapeutic expertise and knowledge of the clinical research landscape
- Ability to acquire and maintain expertise to support portfolio needs
- Legal right to work in the country where the role is based
Benefits
- Medical, Dental & Vision
- Retirement & Pension Plans
- Life Assurance & Disability
- Employee Assistance Programmes
- Wellbeing Resources
- Learning & Development
- Performance Incentives
Company overview
ICON plc is a global leader in clinical research and healthcare intelligence, founded in Dublin, Ireland in 1990. As one of the world's largest contract research organizations (CROs), ICON provides comprehensive outsourced development services to pharmaceutical, biotechnology, and medical device companies worldwide. The company operates in 55 countries with approximately 41,900 employees, offering end-to-end solutions that span the entire product development lifecycle. ICON's service portfolio includes clinical research services, adaptive trials, biosimilars, commercialization and outcomes consulting, medical imaging, laboratory services, and strategic support for traditional and digital health technologies. The company specializes in therapeutic areas such as oncology, cardiovascular diseases, central nervous system disorders, rare diseases, and women's health. With its 2021 acquisition of PRA Health Sciences, ICON significantly expanded its capabilities and market position, becoming a dominant force in the global CRO industry. The company is publicly traded on NASDAQ under the ticker ICLR and reported $8.28 billion in revenue for 2024.