What are the responsibilities and job description for the Manager, Nonclinical Development position at Kennedy Bond?
Kennedy Bond is partnered with an innovative, clinical stage Neurology focused Biotech in Boston, MA. This is, at least initially, a contract opportunity.
Join a pioneering team at a forefront biotech company in Boston that utilizes groundbreaking scientific approaches to address serious neurological conditions. We are on the lookout for a skilled Manager in Nonclinical Development to become a vital part of our dynamic and innovative team.
In this essential position, you will strategize, coordinate, and oversee nonclinical safety programs, ensuring adherence to regulatory and project goals. You will need to engage with various functions and manage relationships with outsourced CROs to foster scientific rigor and operational excellence from discovery to clinical development.
Ideal candidates will have:
- A master's or doctoral degree in a life science field.
- 5 years of experience focused on nonclinical safety/toxicology, successfully managing outsourced studies.
- Proven experience with IND or equivalent global regulatory submissions.
- Comprehensive understanding of global regulatory guidance.
- Strong skills in managing CROs, collaborating across functions, and solving complex problems.
- Flexibility and determination to succeed in a fast-paced, collaborative biotech environment.
If you’re eager to contribute to a company that’s leading the way in the treatment of neurological diseases, we’d love to connect with you!