Director, Clinical Regulatory - South San Francisco

We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients. · ...

Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. · ...

We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients. The Associate Director, Clinical Regulatory is a highly motivated and creative individual with deep and broad regulatory experience and expertise. · Ac ...

Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. · ...

We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients. · The Associate Director, Clinical Regulatory is a highly motivated and creative individual with deep and broad regulatory experience and expertise. · ...

+Job summary · Senior Advisor, Regulatory and Clinical Affairs at ZEISS. · +ResponsibilitiesProvide input to regulatory and clinical strategies of all CZM products for the US market. · Participate in strategy and management meetings. · ...

The Senior Advisor, Regulatory and Clinical Affairs, · US is responsible for guiding regulatory and clinical strategies to ensure an optimized, · successful, timely and resourceful commercialization of CZM's global product portfolio in the United States.This role acts as an advis ...

This leadership role is responsible for developing and implementing global regulatory strategies for clinical investigational studies and commercialization of vaccines for both adult and pediatric populations. · In collaboration with Clinical Development and Safety this role is r ...

+ Develop and implement globally viable clinical regulatory strategies+ Ensure adherence to current regulatory requirements and alignment with appropriate regulatory guidance (including ICH) and industry best practices+ Serve as a primary point of contact with regulatory authorit ...

Nura Bio is a clinical-stage biopharmaceutical company developing neuroprotective therapies for the treatment of neurological diseases. · ...

+Job summary · Reporting to the Chief Medical Officer (CMO), the Vice President, Clinical Development provides executive leadership for the company's clinical research and development activities within designated therapeutic areas and/or programs. · +QualificationsM.D. degree; ad ...

We are currently hiring a Director CMC Regulatory Affairs to join our Technical Operations team. · ...

Join Maze Therapeutics as an Associate Director, Regulatory Affairs. · Represent Regulatory Affairs for assigned programs. · Contribute to the development and implementation of regulatory strategies for assigned programs. · ...

We are seeking a Senior Manager to join our regulatory affairs team. You will provide regulatory expertise and executional leadership for our clinical-stage programs. · ...

The Associate Director of Regulatory Affairs will play a critical role in advancing clinical-stage programs by providing regulatory expertise and executional leadership. · ...

Join Maze Therapeutics as a Senior Manager, Regulatory Affairs. · ...

The Position: · Join Maze Therapeutics as an Associate Director, Regulatory Affairs. · ...

Join Maze Therapeutics as a Senior Manager, Regulatory Affairs. · Represent Regulatory Affairs for assigned programs · Support the development and implementation of regulatory strategies for assigned programs in alignment with corporate objectives and regulatory requirements · ...

Lycia Therapeutics is seeking a Director or Associate Director of Clinical Science who will play a critical role in the design, execution, and analysis of clinical trials of clinical stage assets. · ...

We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. · Lead the medical writing function. · Author and review clinical and regulatory documents. · Collaborate with cross-functional p ...