Director, Scientific Operations - {{In Vivo Study Operations and CGT}}

RPM ReSearch
  • California
    30+ days ago

    Job Description

    Scientific Director- In Vivo Study Operations and CGT


    Location: San Diego/Carlsbad, California 


    If you are looking for a scientific leadership position of a multidisciplinary cross-functional, in vivo scientific team spanning several disciplines, you should consider acting as a subject matter expert in Cell and Gene Therapy (CGT) and a leader of the study directors in the largest in vivo site of our organization. This role will be responsible for the oversight of scientific operations spanning both tactical planning and strategic vision. 


    In this role, you will:

    • Provide technical leadership and technical direction for in vivo effectiveness and toxicology CGT studies at preclinical programs.
    • Guide and Mentor CGT Study Directors, as well as others, and may serve as Study Director for in vivo CGT studies as needed, especially in client communication and questions.
    • Manage scientific expectations of a cross-functional multidisciplinary group of 8 Ph.D. scientists.
    • Provide guidance for Study Director in other focus areas
    • Recommend and implement techniques to increase productivity, increase efficiency, leverage opportunities, and maintain state-of-the-art processes.
    • Works with Quality Assurance department on regulatory updates of GLP requirements as they apply to contracted studies within the organization. 
    • Works within the operations and business development team to increase external awareness and exposure of company capabilities for in vivo CGT and complimentary service offerings. 


    Experience

    • A minimum of 10 years of experience in a GLP-regulated environment in the biotechnology, toxicology, pharmaceutical, or related industries.
    • CRO experience is highly desired, and/or experience performing in a setting of managing client deliverables. 
    • Experience conducting in vivo GLP studies related to Cell and Gene Therapy
    • Experience having taken a drug product or device through pre-IND enabling phases


    Education

    • (DABT) Board Certification in Toxicology or eligibility is highly desired
    • Ph.D. in cell biology, immunology, pharmacology, toxicology, or relevant scientific discipline


    This position is a full-time permanent position that requires onsite presence. There can be times when a day or two of working from home is possible close to the location once acclimated to the role. 



    Numbers & Facts

    LocationCalifornia

    Skills

    • Biotech and Pharmaceuticalunmatched
    • Business Developmentunmatched
    • Cell Biologyunmatched
    • Contract Research Organization (CRO)unmatched
    • Cross-Functionalunmatched
    • Delivery Managementunmatched
    • Drug Productsunmatched
    • GLP (Good Laboratory Practices)unmatched
    • Gene Therapyunmatched
    • Immunologyunmatched
    • Insurance Regulationsunmatched
    • Investigational New Drug (IND)unmatched
    • Leadershipunmatched
    • Mentoringunmatched
    • People Managementunmatched
    • Pharmacologyunmatched
    • Pre-Clinical Trialsunmatched
    • Productivity Managementunmatched
    • Quality Assuranceunmatched
    • Sales Managementunmatched
    • Strategic Planningunmatched
    • Tactical Operationsunmatched
    • Technical Leadershipunmatched
    • Toxicologyunmatched
    • Toxicology Researchunmatched

    Be found by employers

    5,500+ employers search our resume database daily. Add yours to get found by recruiters looking for candidates like you.

    Level up your application

    Professional resume templates

    Browse dozens of recruiter approved resume templates, layouts and formats. Choose your favorite and make it your own in minutes.

    Free resume templates

    Free resume builder

    Improve your existing resume or start from scratch and create a standout, ATS-friendly resume. Add job-specific content, download and apply.

    Free resume builder