New York, New York
Molecular Templates, Inc.
Molecular Templates is a clinical stage biopharmaceutical company focused on the discovery and development of differentiated, targeted, biologic therapeutics for cancer. We believe our proprietary biologic drug platform technology, referred to as engineered toxin bodies, or ETBs, provides a differentiated mechanism of action that may address some of the limitations associated with currently available cancer therapeutics. ETBs utilize a genetically engineered form of Shiga-like Toxin A subunit, or SLTA, a ribosome inactivating bacterial protein, that can be targeted to specifically destroy cancer cells. Additional information about Molecular Templates can be obtained at .
The Manager serves as the Regulatory Lead for products while managing, reviewing, planning, and preparing complex regulatory submission documents for global regulatory filings. Among other responsibilities, the Manager will interpret regulations, and provide regulatory guidance to global regulatory teams. The Manager has the authority to submit complex submissions and may act as primary MTEM contact with US FDA and may lead selected US FDA meetings while ensuring technical accuracy and regulatory compliance of submissions.
Reporting Structure: This position will not have supervisory responsibilities. This position reports to VP of Regulatory Affairs.
Molecular Templates, Inc. is an Equal Opportunity Employer and offers competitive salaries and benefits.
Molecular Templates Inc
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