Neurological Surgery Clinical Research Assistant II-Onsite

Ohio State University; New Albany (IN); On-site; USD 48,000 - 72,000; Full time

Benefits offered by this job

Comprehensive benefits

Onsite role with travel to OSU sites

Job summary

The Ohio State University is seeking a Clinical Research Assistant 2 in Neurological Surgery. This onsite role involves coordinating and performing clinical research tasks, including patient interactions, data handling, and collaboration with the COM Center for Clinical Research Management.

A bachelor’s degree in related sciences is required, with 2–4 years of experience preferred. You will assist with IRB documentation, patient recruitment, informed consent, testing, data entry, and preparation

Qualifications

• Bachelor's degree in biological, health, or medical sciences or equivalent experience.
• No prior experience is required, though 2–4 years of relevant experience is preferred.
• Proficient computer skills are essential.
• Experience in research settings and knowledge of clinical protocols may be desired.

Responsibilities

• Coordinate and perform data collection, maintenance and reporting for clinical studies.
• Identify and recruit eligible participants; obtain informed consent and educate participants on the study process.
• Coordinate patient appointments and procedures; administer standardized testing and calculate scores.
• Collect, process and evaluate biological samples; assist with data entry into study databases.
• Prepare documentation for progress reports; assist with IRB and sponsor study documents; support manuscripts and grant proposals.

Skills

Clinical research coordination

IRB documentation

Informed consent

Data entry

Education

Bachelor's degree in biological, health, or medical sciences

Tools

MS Office

Job description

The Ohio State University is seeking a Clinical Research Assistant 2 in Neurological Surgery. This onsite role involves coordinating and performing clinical research tasks, including patient interactions, data handling, and collaboration with the COM Center for Clinical Research Management.

A bachelor’s degree in related sciences is required, with 2–4 years of experience preferred. You will assist with IRB documentation, patient recruitment, informed consent, testing, data entry, and preparation