Senior Preclinical Research Manager

3 weeks ago


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

At S3 Science, we are seeking a highly skilled Preclinical Study Director to lead our preclinical research efforts. 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 that study protocols are aligned with company goals and comply with GLP and regulatory requirements.
  • Serve as the main point of contact and scientific lead for preclinical studies, ensuring smooth coordination with internal teams and external CROs.
  • Oversee the collection, analysis, and interpretation of preclinical data, ensuring the scientific quality and integrity of results.
  • Prepare and review comprehensive study reports, ensuring accuracy, completeness, and adherence to regulatory requirements.
  • Lead cross-functional project teams, including toxicologists, pharmacologists, lab technicians, and external collaborators.
  • Act as a liaison between the preclinical research team and other departments such as clinical development, regulatory affairs, and quality assurance.
  • Ensure all studies are conducted in compliance with Good Laboratory Practice (GLP) regulations and other relevant regulatory guidelines.

Requirements:
  1. PhD in Pharmacology, Biology, or related scientific field (Master's degree with significant relevant experience may be considered).
  2. Minimum of 4 years of experience in preclinical research within the pharmaceutical or biotechnology industry.
  3. Strong scientific knowledge in pharmacology, toxicology, or related disciplines.
  4. Excellent project management skills with the ability to manage multiple studies simultaneously.


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