Assistant Study Coordinator (LAUNCH Program) - Ophthalmology

As the Assistant Study Coordinator for the LAUNCH program, you will assist the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. In this role, you will recognize and perform necessary tasks to assist the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in managing projects and prioritizing work to meet necessary deadlines. You will support the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations. Thefullsalary range for this position is $27.08 - $43.55/Hourly. The budgeted salary that the University reasonably expects to pay for this position is $27.08/Hourly.

This is one of six open positions. By applying to this posting, you'll be considered for all available opportunities.

Please note that this is a full-time 12-month limited position and may convert to career.

Salary Range: $27.08 - $43.55/Hourly

• Minimum of 1+ years of experience in a clinical research setting.
• Interpersonal skillstoeffectively communicate information in a timely, professional manner andestablish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators, and administration and to work as a member of a team.
• Ability to effectively communicate to and interact with patients in a compassionate and kind manner.
• Ability to set priorities and complete ongoing tasks with competing deadlines to meet the programmatic and department needs while complying with applicable University policies and federal and state regulations.
• Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.
• Closeattentionto detailto ensure accuracy in a fast-paced, fluctuating workload environment.
• Organization skillsto create and maintain administrative and regulatory files effectively as well as independently balance the various tasks to ensure deadlines are met.
• Demonstrated proficiency withAdobe and Microsoft suite software, especially Excel, to perform daily tasks efficiently and accurately.
• Alearning and professional growth mentalityso that new software tools, systems, and processes can be adopted quickly and efficiently.
• Workingknowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws.
• Knowledge of and experienceworking with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc.
• Strong verbal and written communication skillsto effectively establish rapport, building collaborative relationships, and communicate complex concepts and ideas in an easy-to-understand manner.
• Ability toadapt to changing job demands and priorities, remainflexibleincluding working flexible hours to accommodate research deadlines.
• Ability to handleconfidential informationwith judgement and discretion.
• High degree ofconcentrationand focusin a work environment that contains distracting stimuli, competing deadlines, and work delegated by more than one individual.
• Availability to work in more than one environment,travelling to various clinic sites, meetings, conferences, etc.

Preferred:

• Bachelor's Degree in related area and/or equivalent combination of education and experience.