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Sutro Biopharma, Inc. is seeking a driven and talented individual to join our Clinical Developmentteam as we change the future of oncology. While collaborating with cross-functional departments, you will play a key role in maximizing our technology and progressing our novel therapeutics. We are dedicated to making a difference in the lives of patients, both as individuals and as part of a team.
This role will be responsible for the development, management, and execution of the GCP QA programs to ensure that all aspects of the drug development process are in accordance with all relevant current FDA and international regulatory guidelines as they pertain to CTI product candidates. The position will also lead all Clinical QA aspects of NDA/MAA/BLA submissions including the development of internal and external audits and training necessary to ensure compliance across the company, and in preparation for all Pre-Approval Inspections (PAI). Reporting to the Chief Medical Officer, this role will partner very closely with Sutro’s Quality group. This position is located at Sutro’s headquarters in South San Francisco, California.
Responsibilities:
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Sound exciting? Apply today and join our team!
Sutro Biopharma, Inc. encourages all colleagues to be fully vaccinated for COVID-19 prior to the first date of employment.
As an equal opportunity employer, we believe in fostering a culture that is inclusive and values diversity in background and opinions. Sutro Biopharma hires extraordinary individuals into every position in the company and is committed to the diversity of our team. Our company progresses without regard of race, ethnicity, gender, sexual orientation, religious belief, age, disability or citizenship status. We are dedicated to creating a safe environment where our employees can grow and succeed together.
We look forward to hearing from candidates who are interested in exploring opportunities with Sutro! Our People & Culture team/hiring managers are unable to respond and do not accept solicitations from third-party agencies.
The anticipated salary range for fully qualified candidates applying for this role at Sutro Biopharma’s California-based locations will be $247,000 – $275,000. The final salary offered will be dependent on several factors that include and are not limited to relevant previous experience, job responsibilities and duration of experience, the type and length of experience within the industry, and education.
About Sutro Biopharma
Sutro Biopharma, Inc., is a clinical-stage company relentlessly focused on the discovery and development of precisely designed cancer therapeutics, transforming what science can do for patients. Sutro’s fit-for-purpose technology, including cell-free XpressCF®, provides the opportunity for broader patient benefit and an improved patient experience. Sutro has multiple clinical stage candidates, including luveltamab tazevibulin, or luvelta, a registrational-stage folate receptor alpha (FolRα)-targeting ADC in clinical studies. A robust pipeline, coupled with high-value collaborations and industry partnerships, validates our continuous product innovation. Sutro is headquartered in South San Francisco. For more information, follow Sutro on social media @Sutrobio, or visit www.sutrobio.com.
Full Time
Pharmaceutical
$174k-220k (estimate)
11/04/2023
06/25/2024
sutrobio.com
SAN CARLOS, CA
200 - 500
2003
Public
EDWARD ALBINI
$50M - $200M
Pharmaceutical
Sutro is a biopharmaceutical firm that develops novel protein and multi-specific antibody-based therapeutics for the treatment of cancer.