Scientific Director of In Vivo Operations

4 weeks ago


San Diego, California, United States RPM Research Full time

As a key member of the RPM Research team, you will lead a multidisciplinary cross-functional in vivo scientific team, providing technical leadership and direction for in vivo effectiveness and toxicology Cell and Gene Therapy studies at preclinical programs.

Responsibilities include guiding and mentoring CGT Study Directors, managing scientific expectations of a cross-functional group of 8 Ph.D. scientists, and recommending techniques to increase productivity and efficiency.

Additionally, you will work with the Quality Assurance department on regulatory updates of GLP requirements and collaborate with the operations and business development team to increase external awareness of company capabilities for in vivo CGT and complimentary service offerings.

Requirements include a minimum of 10 years of experience in a GLP-regulated environment, CRO experience, and experience conducting in vivo GLP studies related to Cell and Gene Therapy.

Board Certification in Toxicology or eligibility is highly desired, as well as a Ph.D. in cell biology, immunology, pharmacology, toxicology, or a relevant scientific discipline.

This is a full-time permanent position that requires onsite presence, with occasional remote work possible once acclimated to the role.



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