The candidate must be entering the first year as an Assistant Professor, will devote 100% effort to clinical trials, and be available by cell phone to field questions from clinical trial participants. The candidate must have prior experience in clinical research in retinal diseases and ocular oncology and be knowledgeable and experienced in each of the following.

(1) Clinical trial design

(2) Study start-up procedures

(3) IRB submissions

(4) Adverse event reporting

(5) Design of source documents

(6) Data entry into iMetadata

(7) Supervising and training study coordinators and post-doctoral fellows

(8) Communicating with sponsors and CRO/CRAs

(9) Interacting with study monitors and overseeing monitoring visits



(10) Experience managing audits by the FDA and EMA

* The referenced salary range reflects base pay, which is based on faculty rank and years in rank. This salary ...