Responsibilities

As a Medical Director/Clinical Trial Physician, you will provide medical leadership to study teams, contributing to the creation of clinical trial protocols and ensuring the reliable and high-quality collection of study data within established timelines and budgets. You will monitor clinical studies in real-time, ensuring medical validity of endpoints and subject safety, while proactively identifying and addressing issues. Additionally, you will interpret clinical trial data for regulatory documents, prepare medical materials for stakeholders, and serve as a medical point of contact for internal and external parties, including investigators and health authorities. You will also ensure study compliance by adhering to SOPs and GCP guidelines, collaborating with site staff, and providing medical training.