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An exciting and innovative clinical-stage biopharmaceutical company dedicated to the development of first-in-class cellular immunotherapies for patients with cancer and autoimmune disease is looking for an Associate Director in Regulatory Affairs to oversee and contribute to the strategic planning and execution of clinical regulatory activities essential for initiating and conducting clinical trials and securing marketing authorization. This role involves extensive interaction with regulatory agencies such as the FDA, EMA, and PMDA, seeking scientific advice and approvals, and provides cross-functional leadership for global filings, ensuring compliance with local regulatory requirements and authoring/reviewing submission documents for regulatory applications. The ideal candidate will have experience leading regulatory teams and a successful record of approved regulatory submissions. This is a full-time, exempt position located at our corporate headquarters in San Diego, CA.
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Full Time
$152k-202k (estimate)
06/14/2024
07/02/2024
partnology.com
San Diego, CA
The following is the career advancement route for Associate Director Regulatory Affairs positions, which can be used as a reference in future career path planning. As an Associate Director Regulatory Affairs, it can be promoted into senior positions as a Regulatory Affairs Director that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Associate Director Regulatory Affairs. You can explore the career advancement for an Associate Director Regulatory Affairs below and select your interested title to get hiring information.