Clinical Trials Project Manager: Patient-Centric Research

PRC Prairie Education and Research Cooperative; Springfield (IL); On-site; CAD 55,000 - 83,000; Full time

Benefits offered by this job

Comprehensive benefits package

Education assistance up to $5,250/year

Adoption assistance up to $7,500

PTO & leave benefits

Retirement benefits

Job summary

Hospital Sisters Health System seeks a Project Manager-Clinical Trials to oversee management of multiple trials, including patient selection, consent, data collection, and adverse event reporting. The role acts as a liaison among patients, families, and healthcare professionals, ensuring protocol compliance across sites.

Requirements include a bachelor's degree in a healthcare field (master’s preferred) and 2 years of clinical research experience; CITI training within 30 days and BLS may be

Qualifications

• 2 years healthcare or clinical research experience required.
• Clinical research professional certification is preferred within 3 years of employment.
• Training in Human Subject Protection and Good Clinical Practices (CITI) required within 30 days of hire.
• Illinois Basic Life Support (BLS) preferred.

Responsibilities

• Manage multiple clinical research trials and coordinate patient enrollment.
• Obtain informed consent and document all required case report forms.
• Identify potential adverse events and report to appropriate bodies.
• Ensure site/principal investigator compliance with approved protocols.
• Act as liaison between patients, families and healthcare professionals.

Skills

Clinical research experience

CCRC certification

Informed consent process

Education

Bachelor’s degree in nursing/science/healthcare related field

Master’s degree in healthcare/research/business

Associate’s degree in radiology + 3 years experience (alternative)

Job description

Hospital Sisters Health System seeks a Project Manager-Clinical Trials to oversee management of multiple trials, including patient selection, consent, data collection, and adverse event reporting. The role acts as a liaison among patients, families, and healthcare professionals, ensuring protocol compliance across sites.

Requirements include a bachelor's degree in a healthcare field (master’s preferred) and 2 years of clinical research experience; CITI training within 30 days and BLS may be