Senior Clinical Scientist - Early Development Lead

ICON

Reading

On-site

GBP 70,000 - 110,000

Full time

14 days+
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Benefits offered by this job

Annual leave
Health insurance
Retirement planning
Employee assistance program
Life assurance

Job summary

ICON Strategic Solutions in Reading, United Kingdom, is seeking a Senior Clinical Scientist to design and conduct clinical studies evaluating the safety and efficacy of innovative treatments. The role emphasizes strategic leadership across early clinical development and clinical pharmacology, with collaboration across physicians, statisticians and other critical functions.

You will author protocols, analysis plans, and regulatory submissions, ensure timely delivery within budgets, and contribute

Qualifications

  • PhD/MD/PharmD or 10+ years in early development/clinical pharmacology.
  • Experience in early phase/Phase I studies.
  • Clinical pharmacology, immunology or oncology experience preferred.
  • Ability to analyze problems and propose creative solutions.

Responsibilities

  • Provide strategic leadership for clinical programs in early development.
  • Maintain knowledge of competitive landscape and cross-functional support.
  • Author/review protocol, analysis plans, and regulatory submissions.
  • Execute Clinical & Clinical Pharmacology studies with Clinical Operations.
  • Review safety/efficacy data with Medical Monitor.
  • Collaborate with Quantitative Clinical Pharmacology and Statistics.
  • Contribute to program strategy and clinical development plans.
  • Draft/Review INDs, amendments, Investigator Brochures, annual reports.

Skills

Strategic Leadership
Clinical Pharmacology
Early Phase/Phase I
Immunology
Oncology

Education

PhD
MD
PharmD
BS/MS in related discipline

Job description

ICON Strategic Solutions in Reading, United Kingdom, is seeking a Senior Clinical Scientist to design and conduct clinical studies evaluating the safety and efficacy of innovative treatments. The role emphasizes strategic leadership across early clinical development and clinical pharmacology, with collaboration across physicians, statisticians and other critical functions.

You will author protocols, analysis plans, and regulatory submissions, ensure timely delivery within budgets, and contribute

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