Under the direction of the Principal Investigator and the senior Project Manager, the Project Coordinator will help manage tasks contributing to the success of research projects conducted in the offices of Dr. Beate Ritz. Coordinating research activities related to study planning, development, monitoring, and implementation, with tasks including, but not limited to, protocol development, protocol submission, IRB materials submission, IRB management, field work planning, organizing research materials, supervise data entry and interviews with research subjects. Assisting Dr. Ritz in report writing and grant applications.
Percentage of Time:
100
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Shift Start:
8:00 am
Shift End:
5:00 pm
Qualifications for Position
11
Records
Qualifications
Required/Preferred
Must be able to work independently and follow through with assignments with minimal supervision.
Required
Demonstrated excellent written and verbal skills in English.
Required
Experience working in epidemiologic studies
Preferred
Must have valid California driver's license
Preferred
Must have experience conducting detailed health related interviews.
Required
Must have experience working with chronically ill individuals
Required
Ability to keep accurate, detailed and legible records of research data
Required
Ability to work with study participants with respect, sensitivity and maintain confidentiality of participant information
Required
Ability to use personal computer and software such as Excel, MS Word, WordPerfect, MS Access
Required
Willingness to work flexible hours as needed, including occasional weekend hours, as needed for particular research activities
Required
Willingness and ability to drive to field research locations in rural counties
Required
Additional Posting Information
Bargaining Unit:
99-Policy Covered
Application Deadline:
07-14-2023
External Posting Date:
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