10 jobs found in South San Francisco

We are seeking an Associate Director, Medical Writing to lead the development and execution of high-quality clinical and regulatory documentation. This individual will play a key role in shaping document strategy, managing the end-to-end writing process, and ensuring compliance with global regulatory standards. The ideal candidate brings a combination of strong scientific expertise, project leadership, and the ability to collaborate effectively across internal teams, external partners, and vendors. This role requires both hands‑on writing capabilities and the ability to guide complex, cross‑functional initiatives. Key Responsibilities Clinical & Regulatory Writing Leadership Serve as the lead medical writer across one or more clinical programs Author and oversee the development of key clinical and regulatory documents, including: Clinical study protocols and associated documents (e.g., informed consent forms) Clinical study reports (CSRs) Development Safety...

Who We Are Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose mission is to harness advanced technologies and model systems to increase our understanding of the biology that controls human aging. Calico will use that knowledge to devise interventions that enable people to lead longer and healthier lives. Calico’s highly innovative technology labs, its commitment to curiosity-driven discovery science and, with academic and industry partners, its vibrant drug-development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs. Position Description Calico is seeking an Associate Director, Medical Writing to provide leadership and functional oversight for writing and leading the review/approval process of high quality clinical and regulatory documents, in compliance with applicable guidelines and regulations. The successful candidate should be able to effectively collaborate with...

About the job Associate Director Medical Writing Role Overview We are seeking an Associate Director, Medical Writing to lead the development and execution of high-quality clinical and regulatory documentation. This individual will play a key role in shaping document strategy, managing the end‑to‑end writing process, and ensuring compliance with global regulatory standards. The ideal candidate brings a combination of strong scientific expertise, project leadership, and the ability to collaborate effectively across internal teams, external partners, and vendors. This role requires both hands‑on writing capabilities and the ability to guide complex, cross‑functional initiatives. Key Responsibilities Clinical & Regulatory Writing Leadership Serve as the lead medical writer across one or more clinical programs Author and oversee the development of key clinical and regulatory documents, including: Clinical study protocols and associated documents (e.g., informed consent...

Associate Director, Medical Writing South San Francisco, CA – (on-site 4 days/week) The Company: A clinical-stage biotechnology organization focused on aging, and age-related diseases. The Role: The full-time Associate Director, Medical Writing to provide leadership and functional oversight for writing and leading the review/approval process of high quality clinical and regulatory documents, in compliance with applicable guidelines and regulations. The successful candidate should be able to effectively collaborate with cross-functional representatives, collaboration partners, external vendors, and stakeholders while maintaining a positive team environment. This role will function as a strong project manager and technical leader with demonstrated scientific and stakeholder-focused leadership skills. Responsibilities Provides medical writing leadership for clinical programs Acts as a medical writing subject matter expert and collaborates with the Clinical...

About Us Structure Therapeutics develops life‑changing medicines for patients using advanced structure‑based and computational drug discovery technology. The company’s platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinical‑stage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions. Structure Therapeutics is led by an experienced group of international drug innovators and financed by top‑tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and...

Who We Are:Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose mission is to harness advanced technologies and model systems to increase our understanding of the biology that controls human aging. Calico will use that knowledge to devise interventions that enable people to lead longer and healthier lives. Calico’s highly innovative technology labs, its commitment to curiosity-driven discovery science and, with academic and industry partners, its vibrant drug-development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs.Position Description:Calico is seeking an Associate Director, Medical Writing to provide leadership and functional oversight for writing and leading the review/approval process of high quality clinical and regulatory documents, in compliance with applicable guidelines and regulations. The successful candidate should be able to effectively collaborate with cross-functional...

Location: South San Francisco, California, United StatesSalary: $190,000 - $230,000Company: Rigel PharmaceuticalsPosted: 2026-08-18Location: South San Francisco, California, United StatesSalary: $190,000 - $230,000Company: Rigel Pharmaceuticals Inc.Posted: 2026-08-16Position SummaryReporting to the Senior Director of Medical Affairs, this position will be responsible for managing activities essential to the timely execution and tracking of Medical Affairs projects, with a primary focus on the Independent Medical Education (IME) Grants Program and support for Investigator Sponsored Trials (ISTs), Research Collaborations (RCs), and other department operations‑related initiatives.This role will help drive process excellence by collaborating with Medical Affairs colleagues to enhance existing processes and develop new tools, resources, and workflows that support both internal Rigel teams and external partners. The position will also work cross‑functionally with leaders and teams across...

About the job Associate Director Medical Writing Role Overview We are seeking an Associate Director, Medical Writing to lead the development and execution of high-quality clinical and regulatory documentation. This individual will play a key role in shaping document strategy, managing the end‑to‑end writing process, and ensuring compliance with global regulatory standards. The ideal candidate brings a combination of strong scientific expertise, project leadership, and the ability to collaborate effectively across internal teams, external partners, and vendors. This role requires both hands‑on writing capabilities and the ability to guide complex, cross‑functional initiatives. Key Responsibilities Clinical & Regulatory Writing Leadership Serve as the lead medical writer across one or more clinical programs Author and oversee the development of key clinical and regulatory documents, including: Clinical study protocols and associated documents (e.g., informed consent...

About Us Structure Therapeutics develops life‑changing medicines for patients using advanced structure‑based and computational drug discovery technology. The company’s platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinical‑stage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions. Structure Therapeutics is led by an experienced group of international drug innovators and financed by top‑tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and...

Who We Are Calico (Calico Life Sciences LLC) is an Alphabet-founded research and development company whose mission is to harness advanced technologies and model systems to increase our understanding of the biology that controls human aging. Calico will use that knowledge to devise interventions that enable people to lead longer and healthier lives. Calico’s highly innovative technology labs, its commitment to curiosity-driven discovery science and, with academic and industry partners, its vibrant drug-development pipeline, together create an inspiring and exciting place to catalyze and enable medical breakthroughs. Position Description Calico is seeking an Associate Director, Medical Writing to provide leadership and functional oversight for writing and leading the review/approval process of high quality clinical and regulatory documents, in compliance with applicable guidelines and regulations. The successful candidate should be able to effectively collaborate with...