As Medical Manager, You will: 1. Understand the product, protocol and conduct of ophthalmic clinicaltrials in sufficient detail to be able to adequately discuss, direct andmanage task items with the project team members and the study site personnel. 2. Manage modality and project specific training for contract readers. 3. Liaise between MERIT with sponsor company and CROs. 4. Liaise between readers and other functional groups within MERIT. 5. Contribute to the development of imaging procedure documents andimaging and reading charter documents. 6. Perform reading for projects. 7. Perform user acceptance test. 8. Contribute to SEP and/or PSEP documents development. 9. Develop project specific DRP document and manage DRP activities. Qualifications： 1. Education: MD or PhD 2. A minimum of 5 years of ophthalmology research and clinical trial experience. 3. English as the working language, fluent in oral and written English.