Clinical Research Coordinator - Onsite Trials & Compliance

Flourish Research; Milwaukee (WI); On-site; USD 41,000 - 45,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) with employer match

Tuition reimbursement

Parental leave

Employee referral program

Life insurance

Disability insurance

PTO and holidays

Job summary

Flourish Research in Northridge, CA is hiring a Clinical Research Coordinator to support protocol visits, consent, and data entry. This onsite role requires careful documentation, adherence to GCP/IRB, and strong communication with investigators.

Bachelor's degree preferred; 2+ years CRC experience recommended. Competitive benefits include health/dental/vision, 401(k) with match, and PTO. Shift: Monday–Friday, 40 hours weekly.

Qualifications

• Education: Bachelor’s degree preferred; not required.
• Preferably 2+ years’ CRC experience in clinical research.
• Strong knowledge of GCP, IRB, and HIPAA regulations.

Responsibilities

• Read and execute protocol visits and procedures.
• Document assessments, tests, and data per regulations.
• Obtain informed consent and recruit subjects.
• Schedule visits and maintain source documentation.
• Complete case report forms accurately.

Skills

Clinical research methods

Team leadership

Communication skills

Office365

Education

Bachelor's degree preferred

Clinical research experience

Tools

eCRF systems

IRB/GCP knowledge

Job description

Flourish Research in Northridge, CA is hiring a Clinical Research Coordinator to support protocol visits, consent, and data entry. This onsite role requires careful documentation, adherence to GCP/IRB, and strong communication with investigators.

Bachelor's degree preferred; 2+ years CRC experience recommended. Competitive benefits include health/dental/vision, 401(k) with match, and PTO. Shift: Monday–Friday, 40 hours weekly.