Onsite Clinical Research Coordinator — Impact & Growth

Flourishresearch; Chicago (IL); On-site; USD 65,000 - 75,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) match

Tuition reimbursement

Parental leave

Employee referral program

Life insurance

Disability insurance

Paid time off

Job summary

Flourish Research is seeking a Clinical Research Coordinator to perform protocol-specific patient visits, document assessments, obtain informed consent, and recruit eligible subjects in a compliant, ethical, and timely manner. The role requires strong communication, leadership, and problem-solving skills, with daily use of Office365.

The position is onsite in Chicago with a non-exempt classification and a compensation range of 65,000.00–75,000.00, offering health insurance, 401(k) match, and

Qualifications

• Bachelor's degree preferred, however, is not required.
• Preferably a minimum of 2 years’ experience as a CRC, plus 1-3+ years' minimum experience within the field of clinical research or biological research.

Responsibilities

• Read, understand, and can accomplish protocol specified patient visits and procedures.
• Clearly and concisely document patient assessments, observations, test results and other study related information per federal regulations, protocol requirements and GCPs.
• Obtain patient informed consent according to federal regulations, GCPs and IRB requirements.
• Recruit qualified study subjects into assigned protocols to fulfill enrollment obligations within sponsor timelines while following ethics, IRB, GCP and ICH guidelines.
• Complete all required training in a timely manner.
• Schedule and conduct patient visits according to protocol requirements and timelines.
• Maintain accurate and complete written source documentation of patient visits and protocol related activities.
• Accurately complete case report forms (CRFs) and/or worksheets generated by the sponsor.
• Maintain confidentiality of patient and protocol issues per HIPAA and Flourish policies.
• Promptly report adverse events to supervisor and/or PI/Sub-Investigator.
• Report Serious Adverse Events (SAEs) to sponsor within 24 hours of awareness.
• Also report the SAE to supervisor, PI and/or Sub-Investigator.
• Account for clinical trial materials and ensure availability for conduct of the study.
• Maintain ongoing communication with Team Lead I; Team Manager; PI; Sub Investigators and others per protocol requirements and Flourish policies.
• Attend required training courses/conferences to stay abreast of regulatory changes and Flourish policies.
• Pursue educational opportunities to increase knowledge of research processes and regulations.
• Attend Investigator Meetings and/or other training as directed.
• Perform all study-related duties in a time- and cost-effective manner in accordance with Flourish policies.
• Perform all duties safely.
• Represent Flourish Research professionally with staff, sponsors, IRBs, patients/subjects, and medical staff.
• Additional duties as assigned by management.

Skills

Clinical trial procedures

Regulatory compliance

Leadership

Communication skills

Office365

SOP writing/review

Risk analysis

Problem solving

Multi-tasking

Independent thinking

Education

Bachelor's degree preferred

Tools

Office365

Job description

Flourish Research is seeking a Clinical Research Coordinator to perform protocol-specific patient visits, document assessments, obtain informed consent, and recruit eligible subjects in a compliant, ethical, and timely manner. The role requires strong communication, leadership, and problem-solving skills, with daily use of Office365.

The position is onsite in Chicago with a non-exempt classification and a compensation range of 65,000.00–75,000.00, offering health insurance, 401(k) match, and