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Non-Clinical Study Assistant (TEMPORARY)

Location San Rafael, California
BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind.

BioMarin’s Research & Development group is responsible for everything from research and discovery to post-market clinical development. Research & Development involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with rare diseases. Come join our team and make a meaningful impact on patients’ lives. 

The Nonclinical Study Assistant (NSA) is a key support role without Pharmacological Sciences Operations, undertaking essential coordination activities for the study and project teams.


 The NSA will focus on the coordination of activities associated with the management of nonclinical studies and projects under direction, or as delegated by, the RPT Project Manager or Study Monitor.



Study and Project Coordination



    • Execute meeting logistics (e.g., meeting scheduling, minutes, agendas)

    • Submit expense reports and travel coordination for staff

    • Conduct electronic documentation and records management

    • May assist or manage permissions for nonclinical data systems

    • May assist, manage, or maintain department intranet content



Study and Project Activities




    • Facilitate CDA and contract execution

    • Administration of GLP Master Schedule System and maintaining the database in compliance with applicable GLP regulation

    • Assist with regulatory package review

    • Assist in tracking vendor payment, invoices, issues, and escalation

    • File, track, and collate study documentation and samples for archival

    • Assist in study- and program-related data entry and quality control, and study sample coordination

    • Assist with program-related data entry, including programs in the clinical development phase


Cross-functional Representation




    • May assist with cross-functional meeting coordination and minutes


Skills


Microsoft Office (Outlook, Word, Excel, Powerpoint).

Education


BA/BS or higher in nursing, life, health, or data sciences is preferred. Industry or relevant experience in lieu of education is considered.


1 year of experience in the industry or other relevant role.



We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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San Rafael

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