Amgen is seeking a Clinical Trials Regulatory Submission Associate to support regulatory submissions and activities in Argentina. You will work under the Local Regulatory Affairs team to prepare, review, submit, and track essential trial documents, maintain records, and coordinate start-up activities with internal and external partners.
The role requires a Master’s or Bachelor’s with 3+ years in clinical trials, plus 1+ year in regulatory affairs and knowledge of ANMAT/CCIS.