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Head of Pharmacology and Toxicology

2 months ago

King of Prussia, Pennsylvania, United States Franklin Biolabs Full time
Job Title: Head of Pharmacology and Toxicology

Franklin Biolabs is a leading Contract Research Organization (CRO) that has emerged from the esteemed legacy of Dr. Jim Wilson's laboratory. With a rich heritage of over three decades in vector technology, we are poised to redefine the landscape of the global genetic medicines industry.

We are seeking a visionary leader to head our Pharmacology and Toxicology unit. As a key member of our team, you will provide scientific leadership, management, and strategic direction to ensure the delivery of top-quality nonclinical services for clients. Your expertise will be instrumental in guiding cross-functional teams and propelling Franklin's mission to provide high-quality services to further client drug development.

Key Responsibilities:
  • Lead and manage the Pharmacology and Toxicology unit, setting strategic vision and fostering talent development.
  • Line manage staff responsible for Nonclinical Study management, Nonclinical study operations, and Histopathology.
  • Oversee all Pharmacology-Toxicology Unit operations, including resource allocation, budgeting, and operational planning.
  • Ensure high-quality and timely interim and final data reporting to clients.
  • Collaborate with other Unit Heads to plan, formulate, and communicate objectives, creating a shared vision and consistency of procedures across teams and locations.
Qualifications:
  • MD, DVM, or equivalent degree.
  • Ph.D. in a relevant field.
  • 10+ years of relevant histopathology and toxicology experience, including Pharma, Biotech, and/or CRO experience.
  • Board certification by the American Board of Toxicology (ABT) and/or American College of Veterinary Pathologists (ACVP), European College of Veterinary Pathology (ECVP), or Japanese College of Veterinary Pathology (JCVP).
  • Proven management capabilities.
  • Knowledge and experience in GLP and other applicable regulatory requirements.
  • Familiarity with preclinical safety assessment strategies for various drug products, including gene therapy products, small molecules, or other biologics.
  • Excellent verbal and written communication skills.
  • Strong analytical and problem-solving skills.
  • Proficient with Microsoft Office Suite or related software, and with Xybion or other related nonclinical study data capture software.