Founded in 2007, The Oncology Institute of Hope and Innovation (TOI) is advancing oncology by delivering highly specialized, value-based cancer care in the community setting. TOI is dedicated to offering cutting-edge, evidence-based cancer care to a population of more than 1.5 million patients including clinical trials, stem cell transplants, transfusions, and other care delivery models traditionally associated with the most advanced care delivery organizations. With 80+ employed clinicians and more than 600 teammates in 50 clinic locations and growing, TOI is changing oncology for the better. For more information visit www.theoncologyinstitute.com.

This is a fantastic opportunity to join our TOI Clinical Research team!

Description

The Clinical Screener is primarily responsible for screening patients against eligibility criteria in clinical trial protocols and performing duties to support patient randomization into those trials.

Essential Duties and Responsibilities

• Understand clinical trial protocols (rationale, inclusion/exclusion criteria, study design, study medication and comparators, mechanism of action, required procedures, etc).
• Review detailed medical records including electronic medical records, lab reports, biopsies, radiology scans and other related medical data to confirm if a patient is eligible for a clinical trial.
• Liaise with other clinical research staff, medical providers and clinic staff to coordinate screening activities including but not limited to confirming patient eligibility, scheduling consents, placing screening orders, etc.
• Communicate individual patient and study level details with clinical trials sponsors, contract research organizations and other external providers.
• Document patient and study level activities related to screening including patient identifiers, diagnoses, reasons for eligibility, ineligibility, screen failure or confirmations for randomization into clinical trials.
• Performs additional tasks as assigned by clinical research or clinic leadership.

Education:

• Foreign MD graduate or experienced oncology Clinical Research Coordinator preferred
• Bachelor's degree or equivalent required

Skills:

• Proficient in Microsoft Office, Outlook, and other Computer Use
• Ability to organize a high-volume workload and prioritize tasks accordingly
• Strong work ethic and personal integrity
• Timeliness and dependability

Schedule and Location:

• 8 Hour Day Shift, Monday to Friday
• Cerritos, California

Hourly Wage Estimate: $24.00 - $30.00 / hour

The estimate displayed represents the typical wage range of candidates hired. Factors that may be used to determine your actual hourly rate may include your specific skills, how many years of experience you have and comparison to other employees already in this role.