Clin Study Coord I - Ophthalmo

Overview

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.

Responsibilities

MAJOR RESPONSIBILITIES:

-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.

Qualifications

REQUIRED QUALIFICATIONS:

-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

Apply Here: www.click2apply.net/wbkZxDHDyzzrBFDjQf5Lzl

PI208584954