Clinical Research Assistant (Oncology)

SQRL; Los Angeles (CA); On-site; USD 42,000 - 60,000; Full time

Benefits offered by this job

Full benefits package

PTO 15 days

401k with match

Job summary

SQRL is seeking a Clinical Research Assistant to support studies and clinic operations across phases I-IV, with a focus on oncology trials at our Century City site. You will help with patient visits, data collection, consent, and adherence to GCP, IRB, and sponsor protocols while ensuring a high-quality patient experience.

The role requires a Bachelor’s degree (preferred) and at least two years of clinical research experience, with skills in vital signs, phlebotomy, ECG/EKG, and injections.

Qualifications

• Bachelor's degree preferred.
• Minimum of two years of clinical research experience.
• Clinical skills: vital signs, phlebotomy, IVs, injections.
• Familiar with e-source reporting via an electronic platform.
• Strong understanding of ICH, FDA regulations and GCP.
• Excellent communication and interpersonal skills.

Responsibilities

• Support CRCs and site staff with protocol-specified patient visits and procedures.
• Document assessments and study data per regs/GCP.
• Obtain and document informed consent following federal regulations and IRB guidelines.
• Support patient recruitment efforts and scheduling to meet enrollment goals.
• Maintain accurate source documentation and complete case report forms (CRFs).
• Report adverse events to supervisors or investigators as needed.
• Help manage study supplies, lab kits, and other trial materials.
• Maintain confidentiality and follow all applicable compliance and ethical standards.
• Communicate effectively with research team members and document relevant study communication.
• Perform additional duties as assigned by management.

Skills

Clinical research

Vital signs

EKG/ECG

Phlebotomy

Injections

Communication skills

GCP knowledge

Education

Bachelor's degree preferred

Job description

• On-Site in Century City with occasional work days in Panorama City
• Full benefits package including 15 days of PTO and 401k with a match!
• Focus on Oncology Research Trials!

Our Client:

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.

The Role:

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.

• 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,
• etc.Document assessments and study data per regs/GCP
• Obtain and document informed consent following federal regulations and IRB guidelines
• Support patient recruitment efforts and scheduling to meet enrollment goals
• Maintain accurate source documentation and complete case report forms (CRFs)
• Report adverse events to supervisors or investigators as needed
• Help manage study supplies, lab kits, and other trial materials
• Maintain confidentiality and follow all applicable compliance and ethical standards
• Communicate effectively with research team members and document relevant study communication
• Perform additional duties as assigned by management

Qualifications:

• Bachelor's degree preferred
• Minimum of two years of clinical research experience
• Clinical skills preferred: vital signs, EKG/ECG, phlebotomy, and injections
• Familiar with e-source reporting via an electronic platform
• A clear understanding of ICH, FDA, and GCP regulations
• Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral source