Clinical Trials Regulatory Submissions Specialist (Mendoza)

Clinical Trials Regulatory Submissions Specialist (Mendoza)

04 nov
|
Amgen
|
Mendoza

04 nov

Amgen

Mendoza

Amgen SA is seeking a Milestone One Site Coordinator to support trial sites in ICH-GCP compliant activities, within defined timelines and enrollment goals.
You will act as the main liaison between Sponsor/CRO and the site, manage feasibility responses, scheduling, data entry, regulatory documents and site audits, while building strong relationships with sponsors and medical institutions.The role requires a Life Science degree, 3+ years in a clinical trial setting, and upper-intermediate
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📌 Clinical Trials Regulatory Submissions Specialist (Mendoza)
🏢 Amgen
📍 Mendoza

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