• Clinical Research Coordinator

    Actalent (Sacramento, CA)


    Job Title: Clinical Research Coordinator

    Job Description

    We are seeking a dedicated Clinical Research Coordinator to join our prestigious research team. You will play a pivotal role in screening, consenting, and enrolling patients in oncology trials, as well as managing their journey through the course of therapy. This patient-facing role involves extensive collaboration with clinical staff to ensure protocol compliance and the successful execution of research procedures.

    Responsibilities

    + Screen, consent, and enroll patients on oncology trials, ensuring protocol compliance.

    + Document patient interactions and procedures in the Electronic Medical Records (EMR) system.

    + Order labs and manage source documentation for patient trials.

    + Collaborate with clinic staff to schedule patient appointments, such as EKGs and vitals.

    + Interact with nursing staff and medical assistants to ensure seamless patient care.

    + Work with infusion nurses to coordinate appointment schedules.

    + Assist with pre-screening patients, chart reviews, and patient recruitment.

    + Provide patients with a personalized calendar of events and study checklists.

    + Identify and manage potential side effects in oncology patients.

    Essential Skills

    + Minimum of 2 years of experience as a Clinical Research Coordinator (CRC).

    + Proficiency in clinical research, pre-screening patients, and patient recruitment.

    + Strong organizational skills and ability to read and interpret clinical protocols.

    + Bachelor's degree in a related field.

     

    Additional Skills & Qualifications

     

    + Experience with patient study enrollment and managing study requirements.

    + Ability to assist patients with trial participation aspects.

    + Knowledge of oncology patient care and support during therapy.

    Work Environment

    Join one of the 41 comprehensive cancer centers, renowned for cutting-edge research and novel treatments. Work with dedicated investigators in a collaborative and supportive environment. Trials include pharmaceutical sponsor-led studies and investigator-led projects, with a mix of federal, institutional, and industry sponsorships. Disease teams are determined by candidate experience and business needs. Work schedule is Monday to Friday, 8 AM to 5 PM, with some flexibility. The role requires on-site presence for clinic visits, providing an opportunity to work closely with clinical and data management teams.

     

    Job Type & Location

     

    This is a Contract to Hire position based out of Sacramento, 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 remote position.

     

    Application Deadline

     

    This position is anticipated to close on Jan 30, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    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 due to a disability, please email [email protected] (%[email protected]) for other accommodation options.