Regulatory Assistant
Actalent•Saint Louis, MO
369d•$20 - $20•Hybrid
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About The Position
Assist other regulatory coordinators with their duties, focusing primarily on pharmaceutical sponsor studies. This role involves handling administrative work for ongoing and continuing studies in medical oncology. The work will be organized through request forms and involves collaboration with PIs, clinical coordinators, and the IRB to ensure regulatory documents are approved and accurate. Note that there is no patient or clinic interaction involved in this position.
