Part-Time
Cello Therapeutics, Inc. is a rapidly growing biotech company located in the Sorrento Valley—one of the major biotech hubs in the nation. Cello focuses on the development of novel nanotherapeutics based on biomimetic cell membrane-coated nanoparticles for cancer treatment. Cello offers a highly motivational and rewarding working environment with attractive salary and benefits.
The Senior Regulatory Consultant will be a key leader of our teams and will provide management and leadership for Regulatory Affairs to support the development and implementation of regulatory strategies and processes associated with cancer treatment products. This includes formulating and implementing CMC regulatory strategies for the development of novel nanomedicines for cancer treatment, provide guidance for CMC regulatory activities in line with US or ICH requirements, and working with partners to facilitate co-development and approvals. The Senior Regulatory Consultant will work closely with many different teams (i.e. R&D, Product Development, CMC, Quality, etc.) to ensure cohesion of regulatory strategy, regulatory requirements, and timely, compliant submission and approval of regulatory filings. Primary duties include:
Successful candidate must be authorized to work in the United States.
Cello Therapeutics, Inc. is an equal opportunity employer.
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