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Job Title: Clinical Research Coordinator

Job Description

Join a leading medical team as a Clinical Research Coordinator, where you will play a crucial role in patient-facing activities. This includes screening, recruitment, managing source documentation, and documenting in electronic medical records (EMR). You will be responsible for specimen collection, ordering labs, and overseeing the enrollment and follow-through of oncology trials.

Responsibilities

+ Screen, consent, and enroll patients on oncology trials, following them through their therapy course.

+ Spend most of the time in the clinic, seeing patients with doctors and attending patient visits.

+ Ensure questionnaires are completed and research procedures outside clinical norms are conducted.

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

+ Ensure protocol compliance by maintaining correct timeframes.

+ Interact with nursing staff and medical assistants.

+ Collaborate with clinical staff to obtain insurance authorizations.

+ Work with infusion nurses to schedule appointments.

+ Support the clinical side of patient therapy.

Essential Skills

+ Minimum 1.5-2 years of experience as a Clinical Research Coordinator.

+ Experience with clinical research, pre-screening patients, oncology, and chart review.

+ Experience in patient recruitment, screening, consenting, and source documentation.

+ Patient study enrollment experience with a focus on drug studies.

+ Experience processing blood and human specimens.

+ Ability to work with drug/interventional studies.

Additional Skills & Qualifications

+ Phlebotomy skills are a plus but not required.

+ Experience in infectious disease, nephrology, allergy and immunology, and endocrinology is beneficial.

+ Attitude and enthusiasm are highly valued.

Pay and Benefits

The pay range for this position is $30.00 - $38.00/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 Sacramento,CA.

Application Deadline

This position is anticipated to close on Sep 15, 2025.

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.