Onsite Oncology Trials Coordinator - Lead Protocols

Advocate Health; Crystal Lake (IL); On-site; USD 60,000 - 85,000; Full time

Job summary

Advocate Health is seeking an onsite Research Coordinator to coordinate clinical trials and related studies. You will guide physicians, staff, and sponsors, ensuring adherence to protocols and regulatory requirements across sites.

The role requires 2 years of research experience and a strong background in GCP/ICH, with proficiency in EMR and MS Office. Collaboration with investigators and a commitment to quality and patient safety are essential.

Qualifications

• Bachelor's degree in biology/health science/nursing or related field is required.
• Typically 2 years of experience in research.
• Knowledge of Good Clinical Practices, ICH guidelines and FDA regulations.

Responsibilities

• Performs clinical and administrative coordination of sponsored clinical trials and related studies.
• Coordinates study start-up, IRB submissions, recruitment and enrollment activities.
• Ensures specimen collection, processing and shipment meet laboratory requirements.

Skills

Communication skills

Time management

Mentoring

Attention to detail

Problem solving

Interpersonal skills

Education

Bachelor's Degree in Biology

Bachelor's Degree in Health Science

Bachelor's Degree in Nursing or related field

Tools

EMR

Microsoft Office

Job description

Advocate Health is seeking an onsite Research Coordinator to coordinate clinical trials and related studies. You will guide physicians, staff, and sponsors, ensuring adherence to protocols and regulatory requirements across sites.

The role requires 2 years of research experience and a strong background in GCP/ICH, with proficiency in EMR and MS Office. Collaboration with investigators and a commitment to quality and patient safety are essential.