Job Description

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Job Title:Clinical Research Assistant - Comprehensive Cancer Center

Department:Medicine | IM Administration

Position Summary

This position supports human laboratory studies examining how nicotine product design influences product abuse potential. The role contributes to advancing scientific knowledge and supports clinical research aimed at improving public health. The Clinical Research Assistant works closely with study participants, study investigators, and a multidisciplinary research team to ensure high-quality data collection and adherence to study protocols and regulatory requirements.

Responsibilities

• Assist with preparation of study materials, including organizing supplies and setting up laboratory spaces
• Assist with participant recruitment and retention activities
• Assist with screening participant eligibility according to protocol criteria
• Assist with scheduling participant visits and maintaining accurate calendars
• Assist with conducting participant visits and collecting data in accordance with specified clinical research protocols and regulatory requirements
• Assist with maintaining documentation, completing case report forms, and performing data quality control checks
• Assist with coordinating communication among the research team, including investigators, clinical staff, and administrative personnel
• Follow all institutional policies related to human subjects research, safety, and confidentiality

Job Requirements

Bachelor’s degree in Biological Sciences, Health Sciences, or a medically related field, or an equivalent combination of education and experience. Computer skills including experience with Microsoft Office applications.

Preferred Qualifications

One to four years of relevant experience in clinical research, public health research, behavioral science, or human laboratory settings. Familiarity with human subjects research procedures, REDCap, or structured data collection. Strong organizational skills, attention to detail, and effective communication skills. Comfort working directly with study participants and following structured protocols.

Additional Information

Research and Scholarship - Clinical Research - Individual Contributor - Technical - T2 Experienced

Location:Olentangy River Rd, 3650 (2520)

Position Type:Regular

Scheduled Hours:40

Shift: First Shift

Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

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The university is an equal opportunity employer, including veterans and disability.

As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression.

Job Tags

Full time, Work at office, Shift work, Day shift,

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