Clinical Research Assistant (Oncology)

Job Description

Overview:

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• $22 - $32/hr depending on experience

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• Monday-Friday, 8:30 AM - 5 PM (occasional weekends)

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• On-Site in Century City with occasional work days in Panorama City

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• Full benefits package including 15 days of PTO and 401k with a match!

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• Focus on Oncology Research Trials!

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Our Client:

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Our client is a fast growing site network that currently has over 30 sites and constantly expanding! They focus on diversity in their trials including therapeutic areas: oncology, cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. Their sites conduct studies spanning Phases I-IV and they've been awarded for excellence in recruitment and recognized in the industry for retention, a best-in-class experience for patients and sponsors. At this site location, there is a focus on Oncology research trials.

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The Role:

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The Clinical Research Assistant supports clinical research studies and assists with clinic operations and study procedures across all phases of research, ensuring accurate data collection and compliance with GCP, IRB, and sponsor protocols while providing an impeccable patient experience in every, single interaction.

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• Support CRCs and site staff with protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG,

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• etc.Document assessments and study data per regs/GCP

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• Obtain and document informed consent following federal regulations and IRB guidelines

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• Support patient recruitment efforts and scheduling to meet enrollment goals

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• Maintain accurate source documentation and complete case report forms (CRFs)

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• Report adverse events to supervisors or investigators as needed

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• Help manage study supplies, lab kits, and other trial materials

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• Maintain confidentiality and follow all applicable compliance and ethical standards

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• Communicate effectively with research team members and document relevant study communication

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• Perform additional duties as assigned by management

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Qualifications:

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• Bachelor's degree preferred

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• Minimum of two years of clinical research experience

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• Clinical skills preferred: vital signs, EKG/ECG, phlebotomy, and injections

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• Familiar with e-source reporting via an electronic platform

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• A clear understanding of ICH, FDA, and GCP regulations

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• Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral source

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