About the job
Join EyePoint Pharmaceuticals as the Director of Clinical Science, reporting directly to the Chief Medical Officer in a fully remote capacity. In this strategic role, you will lead the advancement of our clinical development initiatives and collaborate with cross-functional teams to shape the future of our product portfolio.
Key Responsibilities:
- Collaborate with cross-functional teams to implement Clinical Development Plans and Registrational Strategies for assigned products.
- Work closely with Clinical Development and Clinical Research Organizations (CROs) to ensure the highest quality of clinical trial documentation, including Clinical Research Protocols, Investigator Brochures, and Clinical Study Reports, in adherence to ICH and GCP standards.
- Facilitate the collection, review, and analysis of clinical trial data, ensuring compliance with statistical analysis plans.
- Conduct ongoing reviews of clinical data to identify trends in safety and effectiveness across trials.
- Prepare clinical documents for submission to global health authorities, including briefing materials for regulatory meetings.
- Contribute to the authorship of meeting abstracts and the publication of clinical trial results.
- Oversee site initiation activities, including the development and execution of monitoring plans.
- Assist in clinical trial recruitment strategies, working with sites to achieve enrollment targets.
- Ensure compliance with global regulatory authority guidelines throughout clinical trial execution.

