Clinical Research Coordinator, Registered Nurse

UroPartners LLC.; Glenview (IL); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a dedicated Clinical Research Coordinator, Registered Nurse. This role involves overseeing study coordination and data management, ensuring compliance with regulatory standards, and advocating for patients. Ideal candidates will possess a BSN and have at least two years of nursing experience in critical care or clinical trials. The position offers competitive pay, generous PTO, and a comprehensive benefits package, making it a fantastic opportunity for those looking to advance their careers in a supportive environment.

Benefits

Health insurance

Dental insurance

Vision insurance

Life Insurance

Pet Insurance

Health savings account

Paid sick time

Paid time off

Paid holidays

Profit sharing

Qualifications

• Minimum 2 years nursing experience, preferably in ICU, ER, oncology, or clinical trials.
• BLS certification required; ACLS preferred.

Responsibilities

• Maintain site compliance with research protocols, laws, and regulations.
• Coordinate patient appointments and collaborate with physicians.
• Educate and ensure protocol compliance among physicians and staff.

Skills

IV Administration

Patient Advocacy

Data Management

Regulatory Compliance

Communication Skills

Organizational Skills

Education

BSN (RN) from an accredited program

Job description

Clinical Research Coordinator, Registered Nurse

Join to apply for the Clinical Research Coordinator, Registered Nurse role at UroPartners LLC.

Work Location

2614 Patriot Blvd (unit A) Glenview, IL 60026

Benefits

• Health insurance
• Dental insurance
• Vision insurance
• Life Insurance
• Pet Insurance
• Health savings account
• Paid sick time
• Paid time off
• Paid holidays
• Profit sharing
• Retirement plan

Job Summary

We offer competitive pay, PTO, holiday pay, and a comprehensive benefits package. Clinical Research Coordinators are responsible for study coordination and data management, focusing on subject recruitment, study implementation, data integrity, and regulatory compliance.

Requirements

Essential Responsibilities

• Maintain site compliance with research protocols, laws, and regulations.
• Stay current with FDA regulations, ICH-GCP guidelines, SOPs, and study protocols.
• Complete required training, including ICH-GCP and IATA certifications.
• Educate and ensure protocol compliance among physicians and staff.
• Develop tools for new protocols and manage complex clinical studies.
• Ensure proper documentation and data management practices.
• Communicate professionally with all stakeholders.
• Act as a patient advocate, providing education and support.
• Coordinate patient appointments and collaborate with physicians.
• Adhere to ethical standards and legal requirements, including HIPAA.

Certifications & Licenses

• BLS certification required; ACLS preferred.
• RN licensure as per state requirements.
• Research certification from SoCRA or ACRP preferred.

Knowledge, Skills & Abilities

• Ability to start IVs, draw blood, and administer IV medications.
• Understanding of biomedical research protocols and regulations.
• Excellent communication, organizational, and computer skills.
• Empathy and ability to build patient relationships.

Education & Experience

• BSN (RN) from an accredited program required.
• Minimum 2 years nursing experience, preferably in ICU, ER, oncology, or clinical trials.

Travel

• May require travel to other sites and meetings.

Physical Demands

Includes lifting, pushing, and pulling within specified weight ranges, with frequency details provided.

Other Details

• Seniority level: Entry level
• Employment type: Full-time
• Job functions: Research, Analysis, IT
• Industry: Medical Practices