Clinical Manager

St. Louis, Missouri Office/Professional 78 days ago

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Summary: Seeking a Clinical Manager with expertise in clinical trials administration and nuclear medicine diagnostics for overseeing study protocols and vendor management.

  • Requirements:

    • BS or MS Degree in scientific or healthcare field.
    • 5+ years of relevant experience with 2+ years in Clinical Trials Administration.
    • Experience in Nuclear Medicine diagnostic and therapeutic clinical trials.
    • Knowledge of FDA regulations, ICH Guidelines, cGCP, and pharmaceutical GXP.

  • Preferred Skills:

    • Experience with CRO/vendor management and budget monitoring.
    • Knowledge of data management/biostatistics processes and pharmacovigilance.

  • Responsibilities:

    • Review study-related documents like protocols, eCRF design, laboratory manuals, etc.
    • Participate in defining and executing the Clinical Study Management Plan.
    • Collaborate with Key Opinion Leaders to integrate feedback into protocols.
    • Contribute to regulatory documents like Investigator's Brochures, IND/NDA submissions.
    • Monitor study progress ensuring compliance with regulations and guidelines.
    • Revise scope of service agreements, budgets, plans with CROs.
    • Perform financial management including review of invoices and site payments.


Pay Details: $115,000.00 to $120,000.00 per year

Equal Opportunity Employer/Veterans/Disabled

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The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance
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