Director Regulatory CMC - South San Francisco

Director Regulatory CMC - Small Molecule & Biologics · Position Description · The Director of Regulatory CMC will lead the development and execution of global CMC regulatory strategies for our pipeline of small molecules and monoclonal antibodies to accelerate clinical developmen ...

The Director of Regulatory CMC will lead the development and execution of global CMC regulatory strategies for our pipeline of small molecules and monoclonal antibodies to accelerate clinical development and ensure seamless commercialization. · ...

The Director of Regulatory CMC will lead the development and execution of global CMC regulatory strategies for our pipeline of small molecules and monoclonal antibodies to accelerate clinical development and ensure seamless commercialization. · ...

Non-Solicitation Policy And Notice To Agencies And Recruiters · IDEAYA's Non-Solicitation Policy strictly prohibits agencies and recruiters from any contact and communication with IDEAYA employees, managers, and leaders to submit unsolicited candidate resumes and/or to solicit bu ...

IDEAYA Biosciences is seeking an experienced leader to head Regulatory CMC. · The Senior Director, Regulatory Affairs CMC will support the CMC Regulatory Affairs function and be responsible for planning and executing the CMC regulatory strategies for IDEAYA's therapeutic developm ...

Non-Solicitation Policy And Notice To Agencies And Recruiters · IDEAYA's Non-Solicitation Policy strictly prohibits agencies and recruiters from any contact and communication with IDEAYA employees, managers, and leaders to submit unsolicited candidate resumes and/or to solicit bu ...

IDEAYA Biosciences is seeking an experienced Senior Director Regulatory CMC to support its therapeutic development programs. · Bachelor's degree in a Life Sciences discipline or equivalent. · Minimum of ten (10) years of experience in clinical regulatory and high potential for le ...

Retro develops therapies for diseases driven by the biology of aging. We focus on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy human lifespan. · We're hiring an experienced CMC Regulatory Lead to o ...

· Retro develops therapies for diseases driven by the biology of aging. We focus on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy human lifespan. · We're hiring an experienced CMC Regulatory Lead t ...

Retro develops therapies for diseases driven by the biology of aging. We focus on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy human lifespan · We're hiring an experienced CMC Regulatory Lead to o ...

Retro develops therapies for diseases driven by the biology of aging. We focus on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy human lifespan. · We're hiring an experienced CMC Regulatory Lead to o ...

Retro develops therapies for diseases driven by the biology of aging. We focus on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy human lifespan. · We're hiring an experienced CMC Regulatory Lead to o ...

· 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 ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS p ...

This is a Regulatory Affairs Manager position supporting preparation review submission CMC sections U.S global regulatory filings INDs CTAs amendments BLAs MAAs coordinating internal stakeholders gather technical information ensure accuracy consistency CMC documentation developin ...

This position supports the preparation review and submission of CMC sections for U.S and global regulatory filings INDs/CTAs amendments and BLAs/MAAs. · ...

Corcept is leading the way in cortisol modulators research. · Lead preparation of CMC regulatory documents; · ...

Corcept is leading the way in the research and development of cortisol modulators. · ...

Senior Manager – Regulatory Affairs CMC · San Francisco, CA · 12+ Months · $100/HR on W2 · *****CANDIDATES SHOULD BE LOCAL AND ABLE TO WORK ON OUR W2***** · Requirements: · Education: BA/BS degree in life science in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engin ...

Provide Regulatory Affairs CMC expertise and leadership for global commercial and development projects. · Provide regulatory strategies, appropriate for the stage of product development, to PSC designed to maximize chances of successful and expedient registration with appropriate ...