Principal Scientist

IREUs, NY
Onsite

About The Position

Principal Scientist; Full-Time; Whitesboro, New York- On-site 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. We are currently seeking a Principal Scientist to join our diverse and dynamic team. As a Principal Scientist at ICON, you will play a pivotal role in leading scientific research and development initiatives that drive innovation and advance clinical programs. You will collaborate with cross-functional teams to design and execute complex studies, provide scientific expertise, and contribute to the development of innovative therapies and solutions that improve patient outcomes.

Requirements

  • Advanced degree in life sciences, chemistry, pharmacology, or a related field (e.g., PhD, MS).
  • Extensive experience in scientific research, drug development, or related areas within the pharmaceutical, biotech, or CRO industry.
  • Proven track record of leading complex research projects, with strong analytical skills and expertise in experimental design, data interpretation, and scientific writing.
  • In-depth knowledge of relevant scientific areas, with the ability to apply this expertise to support clinical and translational research initiatives.
  • Excellent communication and collaboration skills, with experience working in cross-functional teams and presenting scientific findings to diverse audiences.
  • Strong leadership and mentoring abilities, with a commitment to developing junior scientists and promoting best practices in scientific research and development.

Responsibilities

  • Leading the design, planning, and execution of scientific studies, including preclinical, clinical, or translational research, to support drug development programs.
  • Collaborating with cross-functional teams, including clinical, regulatory, and data science, to ensure the integration of scientific insights into clinical trial design and strategy.
  • Providing scientific leadership and expertise in the interpretation of study results, contributing to data analysis, and developing scientific publications and presentations.
  • Identifying and evaluating new technologies, methodologies, and scientific advancements to enhance research capabilities and support innovation in clinical development.
  • Mentoring and guiding junior scientists, fostering a culture of scientific excellence, collaboration, and continuous learning within the team.

Benefits

  • 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
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