Clinical Research Coordinator

Are you an experienced Clinical Research Coordinator looking to take the next step in your career? This is an exciting opportunity to join a growing oncology research program and gain hands-on experience supporting cutting-edge cancer treatment trials. You'll work closely with physicians, patients, sponsors, and research teams to help bring innovative therapies to patients while building specialized oncology research experience.

Responsibilities

• Coordinate all aspects of clinical research studies, ensuring timely and compliant execution from initiation through completion.
• Screen and identify potential study participants, determine eligibility, and facilitate informed consent according to protocol requirements.
• Support and develop patient recruitment and retention strategies to help studies meet enrollment goals.
• Coordinate study visits, specimen collection, processing, and shipment activities.
• Collect, manage, and maintain patient and laboratory data within electronic data capture (EDC) systems and study databases.
• Create and maintain source documents, study trackers, flowsheets, case report forms, and other essential study documentation.
• Ensure protocol compliance and conduct routine reviews of source documentation and case report forms for quality and accuracy.
• Prepare regulatory submissions and maintain IRB approvals, renewals, and essential regulatory files.
• Assemble study materials and kits, coordinate procedures, monitor study-related charges, and serve as the primary contact during sponsor monitoring visits.
• Track study budgets, research-related expenditures, and billing activities in collaboration with finance and leadership teams.
• Partner closely with Principal Investigators and research staff to ensure patient safety, data integrity, and adherence to Good Clinical Practice (GCP) guidelines.
• Maintain complete and accurate research records in accordance with institutional, sponsor, and regulatory requirements.

Requirements

• Required Experience working as a Clinical Research Coordinator (CRC) or in a similar clinical research role.
• Experience with patient screening, chart review, recruitment, and study coordination.
• Working knowledge of clinical trial operations and regulatory requirements.
• Experience with EDC systems and research documentation.
• Preferred Experience supporting oncology clinical trials or oncology patient populations.
• Prior experience with treatment-based oncology studies.
• Strong organizational, communication, and relationship-building skills.

Benefits

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 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)

Pay

The pay range for this position is $30.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Schedule

This is a Contract to Hire, fully onsite position based in Los Alamitos, CA.