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Carle Health · 2 days ago

Clinical Research Coordinator - Oncology

US-IL-Urbana

Full-time

Onsite

Mid Level

$22.40/hr - $37.41/hr

Carle Health is a healthcare system with nearly 16,600 team members in its eight hospitals and various healthcare businesses. The Clinical Research Coordinator (CRC) plays a critical role in the conduct of clinical trials, managing activities from initiation through closure, and ensuring compliance with regulatory standards.

Hospital & Health Care

Responsibilities

Facilitates and coordinates the daily activities of a clinical trial

Conducts clinical trials using good clinical/scientific practices under the auspices of the Principle Investigator and in collaboration with clinical departments and sponsors

Responsible for managing clinical trials from initiation through closure which can include coordinating study development; feasibility evaluation and preparation; IRB submission; recruiting subjects and assessing subject eligibility; reporting of adverse events; data collection and reporting; maintaining regulatory documents; assisting with study modifications; and completing case report forms

Works in collaboration with the Principal Investigator (PI)

Assists Regulatory Specialist in maintaining and retaining regulatory documents in accordance with sponsor requirements

Conducts protocol and feasibility evaluation

Assesses patient population, recruitment and enrollment strategies

Recruits and manages trial subjects to include screening patients for protocol eligibility, covering informed consent, screening and inclusion/exclusion of the subjects adhering to safety and compliance issues

Assists in accurate and timely data collection, collection of source documents documentation, data entry, and reporting

Schedules, coordinates planning and participates in monitoring and auditing activities

Participates in required training and education programs

Assists PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to but not limited to, protocol requirements, schedule of subject visits, execution of research plan. Maintains documentation of training

Maintains effective and timely communications with sponsor, research subjects and PI during the course of the study

Provides a safe environment for patients, families, and clinical staff at all time through compliance with all federal, state, and professional regulatory standards

Reports instances of noncompliance to appropriate institutional oversight body

Maintains strict patient confidentiality according to HIPAA regulations and applicable law

Follows all clinical procedures and guidelines as set forth by regulatory body

Close-out of the clinical trial, contributing to research article, audit preparation, trial closure, communication with authorities and other disciplines involved, assisting in the final study report, completing financial obligations and archives study materials

Qualification

Clinical trial managementRegulatory complianceData collectionPatient recruitmentBachelor's DegreeTrainingEducationCommunication skillsTeam collaboration

Required

Bachelor's Degree: Science

Bachelor's Degree: Health Science

Benefits

Comprehensive benefits package

Company

Carle Health

Glassdoor3.6

Carle Health is a vertically integrated system with a bold but simple mission: to be the trusted partner in all healthcare decisions for everyone who depends on it.

Founded in 1946