Senior Medical Director Sagimet Biosciences Foster City, CA Job Details 22 hours ago Qualifications Medical writing Doctor of Medicine Conference papers Team leadership Scientific and medical presentations experience Scientific research papers Research project design Pharmaceutical company experience Managing clinical research teams Leading team collaboration initiatives Clinical data analysis Pharmaceutical research experience Cross-functional communication Senior leadership Scientific reports Full Job Description As a Senior Medical Director, you will play a critical role in planning and executing Sagimet's clinical trial programs. You will collaborate closely with cross-functional team members, including representatives from Clinical Operations, Regulatory Affairs, Safety Pharmacovigilance, Translational Sciences and Biomarkers, Biometrics, Medical Writing, Research & Development, and Program Management. Your expertise will drive successful planning, execution, analysis and reporting of clinical trials and contribute to the advancement of novel therapies.

Essential Responsibilities:

Clinical Development:

Design, analysis, interpretation, and reporting of clinical trials Medical leadership for the development of clinical study protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions, and other study-related documents Monitor ongoing clinical trials, ensuring adherence to protocols, safety guidelines, and regulatory requirements Review safety events, adverse reactions, and serious adverse events (SAEs)

Collaboration and Leadership:

Work closely with the Clinical Operations team to support trial execution Key medical contact for study investigators, DSMBs, IRBs Provide scientific and strategic leadership, contributing to trial design, endpoints, and patient selection Collaborate with cross-functional team members to develop scientifically sound clinical trial protocols, statistical analysis plans and other study documents that are feasible to execute. Contribute to interactions with regulatory authorities and regulatory submissions Collaborate with study investigators in the preparation, submission, and presentation of scientific data at scientific meets and congresses Maintain current knowledge of therapeutic areas and industry advancements through conferences, literature, and training Represent the company at scientific conferences and engage with key opinion leaders

Requirements Education and Experience:

Medical degree (MD) with board certification, dermatology experience would be a plus 5+ years of experience in clinical development within the biotechnology or pharmaceutical industry with expertise in clinical trial design, execution, and data analysis Expertise in dermatology studies would be a plus Experience in regulatory interactions, submissions, and/or NDA/BLA filings Experience in scientific communication of clinical results through presentations to internal and external audiences, abstracts and publications Excellent verbal and written communication skills, ability to collaborate effectively with thought leaders and investigators Ability to provide scientific and strategic leadership Strong decision-making skills Ability to work in a fast-paced, small company environment with multiple competing responsibilities Position involves 10-20% travel