Clinical Research Coordinator

Clinical Research Coordinator (CRC II / Senior CRC)

We are seeking an experienced Clinical Research Coordinator (CRC) with 3-5 years of experience managing active treatment clinical trials to join a collaborative and highly specialized research team. Oncology experience is preferred, but we are open to candidates with experience in other acute therapeutic areas managing complex interventional studies. This role offers the opportunity to independently manage a portfolio of research participants and protocols while being supported by dedicated Research Assistants and a separate Regulatory Affairs team. The ideal candidate is highly organized, patient-focused, and experienced in coordinating complex study visits from startup through closeout.

Key Responsibilities

• Serve as the primary contact for research participants, sponsors, monitors, and regulatory agencies.
• Independently coordinate assigned clinical studies from startup through closeout.
• Manage a patient caseload of approximately 10-15 active patients across 5-7 protocols.
• Coordinate and conduct approximately 10-12 complex study visits per week.
• Screen, evaluate, and enroll participants according to study protocols and eligibility criteria.
• Obtain informed consent and ensure ongoing participant safety and protocol compliance.
• Collect, process, and coordinate study specimens according to protocol requirements.
• Collect, enter, and manage patient and research data in electronic data capture systems and study databases.
• Complete Case Report Forms (CRFs), source documentation, and study-related records accurately and in a timely manner.
• Review and audit clinical research documentation to ensure completeness, accuracy, and compliance with protocol and regulatory requirements.
• Develop and maintain study tracking tools, flow sheets, recruitment logs, and study documentation.
• Assist with participant recruitment and retention strategies.
• Coordinate study procedures, scheduling, monitoring visits, and sponsor communications.
• Prepare for and participate in sponsor monitoring visits and audits.
• Manage study budgets, monitor expenditures, and collaborate with finance teams to resolve billing questions and discrepancies.
• Partner closely with Principal Investigators to ensure proper study conduct, patient safety, and compliance with GCP, institutional policies, and regulatory requirements.
• Maintain essential regulatory documentation and support IRB renewals and regulatory submissions as needed.

Required Qualifications

• Bachelor's degree in health science, biological science, nursing, or related field preferred.
• 3-5 years of Clinical Research Coordinator experience managing active treatment clinical trials.
• Experience independently coordinating interventional clinical studies.
• Strong knowledge of ICH-GCP guidelines, informed consent processes, and clinical research regulations.
• Experience with clinical trial documentation, source records, CRFs, and data management systems.
• Excellent organizational, communication, and participant management skills.
• Ability to manage multiple protocols and competing priorities in a fast-paced research environment.
• Oncology clinical research experience preferred, but not required.
• Experience working with complex study protocols and high-acuity patient populations.
• CRC, CCRC, or related clinical research certification preferred.
• Experience with sponsor monitoring visits and clinical trial audits.

Job Type & Location

This is a Contract to Hire position based out of Los Alamitos, CA.

Pay and Benefits

The pay range for this position is $30.00 - $40.00/hr. 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)

Workplace Type

This is a fully onsite position in Los Alamitos, CA.

Application Deadline

This position is anticipated to close on Aug 6, 2026.