Director, Clinical Regulatory - South San Francisco

Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of tra ...

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. · ...

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. · ...

+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 ...

· Join our Mission to Protect Humankind · Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to ...

+ 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 ...

Job Summary: · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulat ...

Job Summary · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulator ...

Job Summary · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulator ...

Job Summary · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulator ...

Job Summary · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulator ...

Job Summary: · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulato ...

Key Responsibilities · Clinical strategy & execution · Define and develop the global clinical strategy, aligning with product development, regulatory milestones, and commercialization goals. · Oversee clinical trials, registries, and real-world evidence programs that serve two ke ...

+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 ...

Company Description · ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) ORIC-944, an allosteric inhibitor of the polycomb repressive co ...

· Company Description · ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) ORIC-944, an allosteric inhibitor of the polycomb repressive ...

The Quality Assurance team is seeking a Senior Manager, Clinical Quality Assurance to play a key role in connecting clinical development timelines with essential regulatory and CGP requirements. · In this role, Quality is a proactive partner, not just a checkpoint. You will cont ...