Clinical Research Assistant — Onsite Chicago

Flourish Research; Chicago, Northern (IL, KY); Hybrid; USD 28,000 - 34,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) match

Tuition reimbursement

Parental leave

Employee referral program

Employee assistance program

Life insurance

Disability insurance

PTO and holidays

Job summary

Flourish Research in Chicago, IL is seeking a Research Assistant to support our Ravenswood site. This onsite role involves reading protocols to support patient visits and procedures, documenting assessments, and assisting with recruitment to meet enrollment goals.

Shift is Monday–Friday day shift (40 hours/week). You will obtain informed consent, complete CRFs, and maintain confidential study records while following GCP and IRB requirements.

Qualifications

• Associate degree or adequate experience in clinical research required to compensate.
• Bachelor's degree preferred.
• Experience in clinical research or biomedical research is a plus.

Responsibilities

• Read and understand protocols to support patient visits and procedures.
• Document patient assessments, test results and study data per regulations.
• Obtain informed consent per IRB and GCP requirements.
• Assist in recruitment of qualified subjects to meet enrollment timelines.
• Schedule and conduct patient visits per protocol requirements.
• Maintain accurate source documentation and CRFs/worksheets.
• Maintain confidentiality per policies and agreements.
• Report adverse events to supervisors and PI.

Skills

Clinical research methods

Communication skills

Office365

Education

Associate in science degree

Bachelor's degree preferred

Tools

Office365

Job description

Flourish Research in Chicago, IL is seeking a Research Assistant to support our Ravenswood site. This onsite role involves reading protocols to support patient visits and procedures, documenting assessments, and assisting with recruitment to meet enrollment goals.

Shift is Monday–Friday day shift (40 hours/week). You will obtain informed consent, complete CRFs, and maintain confidential study records while following GCP and IRB requirements.