Crinetics Pharmaceuticals

The Medical Director will lead the design and execution of clinical trials for the endocrinology portfolio, contributing to the Concise Clinical Development Plan (CCDP). They will provide medical monitoring, oversee regulatory documentation, and represent the company to academic and regulatory organizations.

The Senior Medical Director is responsible for developing the clinical strategy and development plans for endocrine disease indications. This includes designing, executing, and analyzing clinical trials and preparing summary documents for global regulatory submissions.

Support the development of drug product formulations from preclinical studies through clinical supply for First-in-Human trials. This includes hands-on laboratory execution, stability testing, and preparing CMC documentation for regulatory submissions.

The Senior Clinical Research Associate oversees clinical trial progress by conducting site visits and ensuring compliance with Good Clinical Practices and study protocols. They collaborate with the study team to manage site relationships, verify data integrity, and resolve performance or compliance issues.