Senior Preclinical Research Manager
3 weeks ago
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:
- 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.
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