Job detail

Clinical Research Asst I

City of Hope

#Regulatory Compliance #Healthcare #Microsoft Office #Data Analysis #Clinical Research #Oncology #Clinical Protocols #Case Report Forms #Cancer Research

Quick overview

Manage multiple oncology clinical research protocols to ensure regulatory compliance and efficient data flow. Coordinate patient recruitment, screening, and specimen collection while collaborating with healthcare professionals.

Requirements summary

Requires a minimum of an Associate's degree, though experience may substitute for education. Candidates must possess strong computer skills and the ability to function independently in a clinical research environment.

associate degreeRegulatory ComplianceSpecimen HandlingData ManagementMicrosoft ExcelMicrosoft WordMicrosoft AccessPatient RecruitmentProtocol DevelopmentClinical Research CoordinationPatient ConsentingCase Report FormsOncology Research

Job description

Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses.
City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix.
Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today.
Develop clinical cancer research protocols under the guidance of a physician.
Manages an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol, attending clinic as needed.
Responsible for compilation, registration and submission of data; monitors and ensures study compliance and maintains a system for effective data flow associated with research protocols.
Schedules patients for biospecimen repository consents, screening, orientation and educational classes.
Meet with and consent patients.
Has proven to function independently and proficiently as defined in the position accountabilities.
Has superb communication and problem-solving skills.
Has demonstrable computer skills in Microsoft Word, Excel, Microsoft Access, etc.
Has undertaken tasks that utilize these computing skills, as well as skills in data management and analyses.
As a successful candidate, you will: Managed multiple oncology clinical research protocols, ensuring compliance with study requirements, regulatory standards, and protocol guidelines.
Coordinated patient recruitment, screening, enrollment, education, scheduling, and registration while maintaining accurate study documentation.
Collected, managed, analyzed, and submitted clinical research data and case report forms according to protocol and sponsor requirements.
Maintained current regulatory and protocol documentation, ensuring readiness for audits and adherence to institutional and compliance policies.
Coordinated protocol-related tests, evaluations, and study activities with physicians, nurses, laboratories, and other healthcare professionals.
Collected, processed, labeled, and transported research specimens while following safety procedures and protocol-specific handling requirements.

Clinical Research Asst I

Clinical Research Asst I

Quick overview

Requirements summary

Job description

Your qualifications should include

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