The Clinical Development Medical Director will lead and provide medical strategic input for clinical program level activities (e.g. submission activities, clinical data review, safety updates, health authority responses, investigator brochure, briefing books etc.) for our clinical trials. The location for this job is flexible between our headquarters in Redwood City, CA, and our lab in Baltimore, MD.
To save sight through transformative science.
We create practical solutions to treat vision-threatening diseases that improve quality of life and care for all involved.
To help people live fuller lives through healthier vision.
- No patient should have to settle for good enough.
- There are no limits to what we can achieve together.
- We are the best when the challenges are big.
- We embrace diversity to enable our success.
“We believe that no patient should have to settle for good enough. We are curious and focused on finding practical solutions that make a real difference.”
- Medical Coverage (Options for HMO, PPO)
- Dental and Vision Coverage
- Life and AD&D Coverage
- Long-Term Disability Coverage
- Short-Term Disability Coverage
- Flexible Spending Account (FSA)
- 401(k) Retirement Plan
- Employee Assistance Program (EAP)
- Additional Life and AD&D Coverage
- Bonus Compensation
- Paid Time Off
- Paid Holidays
The Director, Biostatistics influences and drives statistical strategy and innovation through cross-functional collaboration and decision making. Independently leads quantitative strategy. Represents Biostatistics at internal and external meetings, health authority interactions; Lead statisticians/programmer/s from CROs or hire, develop and mentor statisticians and programmer/s internally; and provide strategic, technical, operational and scientific leadership and solutions to the organization. This job is flexible between our corporate headquarters in Redwood City, CA and our lab in Baltimore, MD.
The Laboratory Technician will work closely with the Research and CMC teams to support the production of novel, sustained-release therapeutic material for the treatment of ocular disease. Responsibilities will range from R&D to GMP work. Day-to-day responsibilities will include equipment setup and operation, record keeping, laboratory cleaning/organization, and waste handling/disposal.