Clin Study Coord I - Ophthalmo

Job Description


GENERAL SUMMARY OF POSITION: Under the direction of the Principal Investigator or designee, the Clinical Study Coordinator I Ophthalmology is responsible for coordinating clinical research studies.



•Collect study data using standardized forms, questionnaires, and other study materials.

•Conduct in-person or telephone interviews with study subjects

•Develop and update spreadsheets

•Track data sent to and returned from study participants using computerized study databases

•Maintain computerized project data files

•Conduct quality control checks for data entry

•Responsible for consistency and accuracy of data entry

•Acquire, download and label imaging data from study sites according to study protocols

•Make calls to acquire off-site data and materials, which may involve minimal evening and weekend times

•Complete information for Internal Review Board, and other regulatory processes

•Assist and provide back-up for Lab duties as needed

•Responsible for coordinating studies according to Study Manuals, updating Manuals, and providing input into improving protocols

•Assist with lab and biorepository tasks

•Collaborate with senior staff and Director on projects

•May help train other study staff

•Perform other duties as required.



•Bachelor’s degree required, preferably in medical sciences or health care field

•0-1 year of related research experience

•Excellent knowledge of computer-based tools (Word, Excel, PowerPoint, etc.) and creating spreadsheets.

•Excellent oral and written communication skills to communicate with patients and offices

•Excellent organization, analytical, and interpersonal skills required

•Superb attention to detail

•Ability to travel to off campus locations

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