Research Assistant
5.
0 Salt Lake City, UT Salt Lake City, UT Part-time Full-time Part-time Full-time $21 - $25 an hour $21 - $25 an hour 16 hours ago 16 hours ago 16 hours ago Duties:
Assist with the screening, recruiting and enrollment of research subjects Perform patient/research participant scheduling Collect patient/research participant history Data entry and Management Adhere to an IRB approved protocol Assist in the informed consent process of research subjects Support the safety of research subjects Coordinate protocol related research procedures, study visits, and follow-up care Comply with organization, and Sponsor policies, standard operating procedures (SOPs) and guidelines Schedule subject visits and procedures Collects, processes and ships laboratory specimens Performs other duties as assigned Qualifications Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines Strong interpersonal skills with attention to detail a must Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems.
Note:
This job description is intended to provide a general overview of the position.
It is not exhaustive or all-inclusive.
Duties and responsibilities may be subject to change based on operational needs.
Job Types:
Full-time, Part-time Pay:
$21.
00 - $25.
00 per hour
Benefits:
Dental insurance Health insurance Paid time off Physical setting:
Clinic Schedule:
Monday to Friday Work Location:
In person.
Estimated Salary: $20 to $28 per hour based on qualifications.
0 Salt Lake City, UT Salt Lake City, UT Part-time Full-time Part-time Full-time $21 - $25 an hour $21 - $25 an hour 16 hours ago 16 hours ago 16 hours ago Duties:
Assist with the screening, recruiting and enrollment of research subjects Perform patient/research participant scheduling Collect patient/research participant history Data entry and Management Adhere to an IRB approved protocol Assist in the informed consent process of research subjects Support the safety of research subjects Coordinate protocol related research procedures, study visits, and follow-up care Comply with organization, and Sponsor policies, standard operating procedures (SOPs) and guidelines Schedule subject visits and procedures Collects, processes and ships laboratory specimens Performs other duties as assigned Qualifications Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines Strong interpersonal skills with attention to detail a must Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems.
Note:
This job description is intended to provide a general overview of the position.
It is not exhaustive or all-inclusive.
Duties and responsibilities may be subject to change based on operational needs.
Job Types:
Full-time, Part-time Pay:
$21.
00 - $25.
00 per hour
Benefits:
Dental insurance Health insurance Paid time off Physical setting:
Clinic Schedule:
Monday to Friday Work Location:
In person.
Estimated Salary: $20 to $28 per hour based on qualifications.
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