Ascendis Pharma is seeking a qualified professional to lead ICSR management in a hybrid Palo Alto setting. The role focuses on processing IC SRS, QA, and cross-functional collaboration to meet safety regulatory requirements. The successful candidate will bring 5+ years of clinical trial and post-marketing case processing experience, working knowledge of safety databases, MedDRA, and regulatory guidelines. Occasional travel up to 20% is required.

Also on the board Same function, level within a rung

Level

Senior

Location

Palo Alto, CA

Occupation

Clinical Research Coordinators

Industry

Pharmaceutical Preparation Manufacturing

Posted

17 days ago

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