Travel Clinical Research Coordinator (Oncology)

Location: Cerritos, CA (Travel to Glendale, Long Beach, Fountain Valley, and Whittier required). Duration: 9-month contract-to-hire.

About The Opportunity

We are seeking an experienced Travel Clinical Research Coordinator (Oncology) to join a growing oncology research program in Southern California. This role offers the opportunity to support approximately 45 active oncology clinical trials while working closely with patients, investigators, sponsors, and a multidisciplinary research team. After initial training in Cerritos, the primary assignment will support the Glendale location, with additional coverage at other sites as needed.

Responsibilities

• Screen, recruit, and obtain informed consent from patients participating in oncology clinical trials.
• Coordinate and manage patient study visits, averaging 2-3 patients per day.
• Perform patient assessments including:
  • Vital signs
  • Phlebotomy
  • ECG/EKG procedures
• Conduct chart reviews to identify eligible patients and verify clinical information.
• Maintain accurate study documentation and ensure protocol compliance.
• Enter study data and resolve queries within Electronic Data Capture (EDC) systems.
• Assist with regulatory documentation and compliance activities.
• Coordinate visit logistics across multiple clinical sites.
• Collaborate with Clinical Research Coordinators, Research Assistants, Data Management, and Regulatory teams.
• Communicate effectively with CROs and study sponsors as needed.
• Ensure patient safety, data integrity, and adherence to study protocols and GCP guidelines.

Requirements

• Minimum of 2 years of Clinical Research Coordinator experience in oncology clinical trials.
• Experience screening, recruiting, and consenting patients.
• Hands-on experience with:
  • Vital signs
  • Phlebotomy
  • ECGs/EKGs
  • Patient study visits
• Strong understanding of oncology clinical research operations and protocol execution.
• Experience reviewing medical records and assessing patient eligibility.
• Excellent organizational, communication, and documentation skills.
• Ability and willingness to travel regularly between Southern California clinical sites.
• Experience with Electronic Data Capture (EDC) systems.
• Experience working with CROs and study sponsors.
• Familiarity with regulatory processes and clinical research compliance requirements.
• Experience working in a multi-site research environment.

Schedule

Monday-Friday | 8:00 AM-5:00 PM

Pay

The pay range for this position is $30-$40/hour, based on experience. Individual compensation within this range will depend on qualifications, skills, relevant experience, job knowledge, geographic location, and internal equity.

Benefits

Eligibility requirements apply to some benefits and may depend on job classification and length of employment. Benefits are subject to change and may include:

• Medical, dental, and vision
• Critical Illness, Accident, and Hospital insurance
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short- and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation, or Sick Leave)