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Senior Medical Director

Jobleads-US

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
  • Collaboration with cross-functional team members to develop scientifically sound clinical trial protocols, statistical analysis plans and other study documents that are feasible, jaum Contribute to interactionsthat goes image or some your security re itself
  • #

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
#J-18808-Ljbffr Jobleads-US
Vacancy posted 1 day ago
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