Clinical Research Assistant

Job Description

Job Description

Job Title: Clinical Research Assistant/Phlebotomist

$20-25/hr --with TONS of career growth opportunity!!

6-month Contract-to-Hire

Must be able to travel to various sites around the LA area as needed

Job Description

The Clinical Research Assistant supports clinical research coordinators in the execution of oncology clinical trials by assisting with patient visits, collecting high-quality data, and contributing to regulatory and data management activities. This role focuses on approximately 45 active oncology trials and is designed as a developmental position that offers a clear path to grow into a Clinical Research Coordinator role.

Responsibilities

• Support clinical research coordinators in the day-to-day conduct of oncology clinical trials.
• Assist with patient study visits, including preparing for appointments, coordinating logistics, and ensuring a professional and compassionate patient experience.
• Perform clinical procedures during study visits, including taking vital signs, conducting ECGs, and performing phlebotomy in accordance with study protocols and site standards.
• Conduct chart reviews and pre-screen patients against protocol-specific eligibility criteria to support enrollment efforts.
• Collect, document, and maintain accurate and timely study data from patient visits and medical records.
• Contribute to data entry into electronic data capture (EDC) systems and support query resolution to ensure data integrity and compliance.
• Collaborate with the data management and regulatory teams to support documentation, regulatory submissions, and ongoing compliance with study requirements.
• Participate in study-related communications with internal teams, contract research organizations (CROs), and sponsors as needed.
• Travel to designated clinical sites for patient visits, following an established schedule provided at least one week in advance.
• Follow all clinical research protocols, standard operating procedures, and ethical guidelines to protect patient safety and confidentiality.
• Actively develop knowledge and skills required to transition into a Clinical Research Coordinator role over time.

Essential Skills

• At least 1 year of experience as a Clinical Research Coordinator or in a closely related clinical research role.
• Hands-on experience participating in or supporting patient visits within clinical research studies.
• Demonstrated ability to conduct study visits, including measuring vital signs, performing phlebotomy, and conducting ECGs.
• Proficiency in chart review and pre-screening patients for clinical trial eligibility.
• Experience with clinical research and clinical trials, preferably in an oncology setting.
• Strong data collection skills with attention to accuracy and detail.
• Certified Phlebotomist with demonstrated phlebotomy competency.
• Ability to travel between multiple clinical sites as required for patient visits.
• Effective communication and interpersonal skills for working with patients and multidisciplinary research teams.
• Strong organizational skills and ability to follow structured schedules and protocols.

Additional Skills & Qualifications

• Oncology research experience is a strong plus.
• Experience with data entry and query resolution in various electronic data capture (EDC) systems.
• Prior experience working with contract research organizations (CROs) and clinical trial sponsors.
• Familiarity with regulatory processes and documentation in clinical research.
• Interest in and motivation to grow into a Clinical Research Coordinator role.
• Ability to work collaboratively within a multi-disciplinary research environment.
• Comfort working in a fast-paced setting with multiple concurrent oncology trials.

Work Environment

The role is part of a collaborative clinical research team that includes full-time and part-time clinical research coordinators, research assistants, data management staff, and regulatory staff providing flexible and corporate support. The team works on approximately 45 active oncology trials, offering exposure to a wide range of studies and procedures. The standard work schedule is 8:00 a.m. to 5:00 p.m. The Clinical Research Assistant trains at the Cerritos site and primarily supports activities in Glendale, with additional travel to sites in Long Beach and Fountain Valley as needed. Work involves direct patient interaction in clinical settings, use of medical equipment for vital signs, ECGs, and phlebotomy, and regular use of electronic data capture systems and other research tools in a professional, detail-oriented environment.

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

The pay range for this position is $20.00 - $25.00/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)

This is a fully onsite position in Cerritos,CA.

This position is anticipated to close on Aug 25, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email View email address on ziprecruiter.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

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Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.