**This is a full-time, long-term position. ** Job Title: Clinical Research Coordinator Company: Ophthalmology Associates Location: Des Peres, MO Travel: Travel to our other clinics in the St Louis metro area and Sullivan, MO will be required as needed. We do pay mileage reimbursement!

Perks

Full

Benefits

Package - Medical, Vision, Dental and Life Insurance 401k + Employer Matching Paid Time Off (PTO) and Paid Holidays Competitive Base Pay Paid Maternity Leave Employee Discounts Hours: Full Time Our offices are open Monday-Friday 8am-5pm You may need to work a little earlier/later as needed JOB SUMMARY The Clinical Research Coordinator provides clinical research support for studies involving human subjects and manages the daily operations of clinical trials. Duties include administration; project implementation, meeting support, quality assurance, and dissemination of results, recruitment; collection, recording, and editing of interview, questionnaire, and clinical data; performing quality assurance monitoring of study data; randomization of study participants; conducting case management tasks; scheduling participant appointments; supporting clinical and group intervention; review medical records following study protocols; and performing other duties in support of clinical trials services as assigned.

RESPONSIBILITIES

Provide assistance in the administrative, technical and scientific day-to-day operation of the study to assure project goals and timelines are met, quality data is collected and managed, and to assure participant and/or data confidentiality. Conduct clinical research as outlined in the study protocol. Maintain knowledge of clinical research issues.

Follow GCP guidelines. Implement confidentiality and privacy regulations. Evaluate protocols, assist in study selection, correspond/coordinate with the sponsor/CRO and prepare study budgets.

Support and assist Research personnel in the operation of equipment used in clinical trials. Support the development of Quality Assurance procedures, and assist with the monitoring of data collection and data transfers. Assist with the preparation of annual IRB reviews.

Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations and/or specific grant/contract language. Understand the operational budget and sub-contracts; track documentation and authorization of payment of study related bills. Provide assistance in the preparation of project reports for PI review and approval.

Recruit study participants to a broad range of studies using specific study protocols to contact, screen, and determine eligibility and schedule appointments with study participants. Collect, edit and record/enter study data via interview, structured interview, questionnaire, medical record review, and basic clinical measurements for complex study protocols, and perform technical duties as assigned. Support orientation and structured intervention sessions in accordance with technical training and certification(s).

Assist with case management activities to support the work of the project(s). Support the process of summarizing and sharing project information with other sites. Support the Project Director, Clinic Coordinator, and/or PI in the maintaining regular contact with other Project Administrators in order to share information and ideas.

Assist with the tracking of papers in process for projects, with planning for project papers and posters to be presented at national and international conferences.

while supporting a culture of high quality and great customer service. Perform other duties in support of clinical trials services as assigned.

QUALIFICATIONS

Demonstrated interpersonal, communica