This role is reporting to the Chief Medical Officer and is remote. Primary responsibilities include, but are not limited to, the following: Individual Responsibilities Contribute in collaboration with a cross‐functional team the implementation of Clinical Development Plans and Registrational Strategies for the assigned products within the portfolio. Collaborate within Clinical Development and partnered Clinical Research Organizations (CROs) on all clinical trial documents including Clinical Research Protocol Synopses, Clinical Research Protocols, Investigator Brochures, Informed Consent Templates, Study Case Report Forms/Electronic Data Capture Systems, Procedure Manuals, Clinical Study Reports ensuring high caliber of all documents in compliance with ICH/GCP standards/Federal and local regulations and company SOPs. Assist in management of the collection, review, and analysis of clinical trial data in compliance with interim analysis and overall statistical analysis plans. Ensure o...