Clinical Trial Research Assistant

IQVIA; Salt Lake City (UT); On-site; USD 36,000 - 89,000; Full time

Job summary

IQVIA is seeking a clinical research support professional in Salt Lake City to assist in the conduct of clinical trials, ensuring adherence to applicable regulations and high quality data management throughout the study.

You will screen and recruit participants, schedule visits, collect histories, input data, coordinate laboratory procedures, and assist with informed consent and safety oversight, while building strong relationships with study teams and investigators.

Qualifications

• High School Diploma or equivalent required.
• Bachelor's Degree preferred.

Responsibilities

• Develop strong working relationships and maintain effective communication with study team members.
• Develop strong working relationships with investigators and office staff to build trust between the clinic and research office.
• Assist with screening, recruiting and enrollment of research subjects.
• Perform patient/research participant scheduling.
• Collect patient/research participant history.
• Data entry and management.
• Coordinate follow up care and laboratory procedures.
• 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 company and Sponsor policies, SOPs and guidelines.
• Schedule subject visits and procedures.

Education

Bachelor's Degree

Job description

IQVIA is seeking a clinical research support professional in Salt Lake City to assist in the conduct of clinical trials, ensuring adherence to applicable regulations and high quality data management throughout the study.

You will screen and recruit participants, schedule visits, collect histories, input data, coordinate laboratory procedures, and assist with informed consent and safety oversight, while building strong relationships with study teams and investigators.