2101 Regulatory Affairs Associate II

Duties:
Assists and coordinates Regulatory Affairs nonclinical / clinical activities related to HA interaction and regulatory submissions throughout the product lifecycle.
Typically, the Associate II will focus on coordinating submission activities and handling routine submissions.

Skills:
Agility and Proactivity, including an ability to recognize, understand, articulate and respond promptly to issues, risks and opportunities that arise.
Communication, including preparing and editing written material that is technically accurate and grammatically correct.
Scientific and Medical Knowledge: Demonstrates basic knowledge of relevant therapeutic area, disease conditions and unmet medical needs.

Education:
Degree in health or life sciences, including chemistry, molecular biology, or similar 0-1+ years with Masters, 2+ with bachelor’s degrees.