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Preclinical Study Director

2 months ago

London, Greater London, United Kingdom S3 Science Full time
Preclinical Study Director

S3 Science is seeking a highly skilled Preclinical Study Director to lead our preclinical research team. As a key member of our team, you will be responsible for overseeing the planning, execution, and reporting of preclinical studies in compliance with regulatory standards.

Key Responsibilities:
  • Ensure study protocols align with company goals and comply with GLP and regulatory requirements.
  • Lead cross-functional project teams, including toxicologists, pharmacologists, lab technicians, and external collaborators.
  • Oversee the collection, analysis, and interpretation of preclinical data, ensuring scientific quality and integrity of results.
  • Prepare and review comprehensive study reports, ensuring accuracy, completeness, and adherence to regulatory requirements.
  • Act as a liaison between the preclinical research team and other departments such as clinical development, regulatory affairs, and quality assurance.
Requirements:
  • PhD in Pharmacology, Biology, or related scientific field (Master's degree with significant relevant experience may be considered).
  • Minimum of 4 years of experience in preclinical research within the pharmaceutical or biotechnology industry.
  • Strong scientific knowledge in pharmacology, toxicology, or related disciplines.
  • Excellent project management skills with the ability to manage multiple studies simultaneously.

About S3 Science:
S3 Science is a leading provider of preclinical research services. We are committed to delivering high-quality results and exceptional customer service. If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply for this exciting opportunity.