Spyglass Pharma

The CRA is responsible for planning, executing, and monitoring clinical trials, including conducting site initiation, routine, and close-out visits. They serve as the primary contact for clinical sites to ensure regulatory compliance and high-quality data entry.

Lead regional medical affairs and scientific engagement to support Phase 3 clinical trial execution and commercialization objectives. Build and maintain strategic relationships with KOLs, healthcare providers, and academic institutions within the ophthalmology space.

Lead regional medical affairs and scientific engagement to support Phase 3 clinical trial execution and commercialization objectives. Build and maintain strategic relationships with KOLs, healthcare providers, and academic institutions within the ophthalmology space.

The specialist will provide hands-on procedural support, real-time coaching, and troubleshooting during implant cases involving the sustained-release drug delivery technology. This role also involves training surgical and clinic staff on device assembly, delivery, integration into workflows, and explaining technology benefits to patients.