Associate Scientific Director

Job Description

Hybrid (3x per week onsite) in Irvine, CA strongly preferred.

Responsibilities

Prepares scientific reports and presentations using available software and templates.

Reviews and contributes to clinical protocols.

Utilizes expertise to assist in interpretation of data.

Brings together all necessary data and information to prepare internal documents or scientific reports; keep multiple reports moving forward simultaneously (multi-tasking).

Coordinates advisory meetings and consulting agreements.

Complies with procedures set forth in relevant IQS documents, study protocols, other directives issued by the management regarding clinical/pre-clinical studies.

Ensures scientific integrity of all processes.

Leads the development of and applies the most current electronic document conventions and processes consistently and accurately.

Provides/presents key clinical study information to therapeutic area and management.

Committed to producing work of the highest quality.

Pays close attention to detail.