Clinical Research Coordinator

Job Title: Clinical Research CoordinatorJob Description

This role offers an opportunity for an experienced Clinical Research Coordinator to support clinical trials at a dedicated research site in Phoenix, AZ. The coordinator will perform hands-on clinical and administrative tasks, including phlebotomy, chart review, and patient pre-screening, while contributing to high-quality clinical research across various therapeutic areas, including oncology.

Responsibilities

• Perform chart reviews to identify and evaluate potential participants for clinical trials.
• Conduct pre-screening of patients to assess eligibility based on study protocols and inclusion/exclusion criteria.
• Support clinical research activities for multiple therapeutic areas, including oncology studies.
• Coordinate day-to-day clinical trial operations in accordance with study protocols and regulatory requirements.
• Assist with patient recruitment by identifying, contacting, and engaging potential participants.
• Perform phlebotomy procedures, including drawing blood samples safely and accurately for study-related testing.
• Collaborate with investigators and clinical staff to ensure accurate documentation and data collection for each study.
• Maintain organized and up-to-date research records, charts, and study documentation.
• Communicate clearly with patients about study procedures, visit schedules, and follow-up requirements.
• Help ensure participant safety and adherence to study protocols throughout the duration of each trial.

Essential Skills

• 2-3 years of experience working as a Clinical Research Coordinator or in a closely related clinical research role.
• Demonstrated phlebotomy experience with the ability to perform blood draws safely and efficiently.
• Proficiency in chart review for identifying eligible patients and extracting relevant clinical information.
• Experience with pre-screening patients for clinical trial eligibility.
• Hands-on experience in clinical research and clinical trial operations.
• Experience supporting oncology clinical trials or working with oncology patient populations.
• Proven ability to recruit and engage patients for participation in clinical studies.
• Strong attention to detail and accuracy in documentation and data handling.
• Ability to follow study protocols, standard operating procedures, and regulatory guidelines.
• Effective communication skills for interacting with patients, investigators, and clinical staff.

Additional Skills & Qualifications

• Certification or training as a Medical Assistant is highly desirable.
• Certification as a Phlebotomist is highly desirable.
• Experience working across multiple therapeutic areas in clinical research.
• Ability to manage multiple tasks and studies in a fast-paced clinical environment.
• Strong organizational skills and the ability to maintain thorough and accurate records.
• Comfort working directly with patients in a clinical research setting.

Work Environment

This position is fully on site at a dedicated clinical research facility in Phoenix, AZ. The coordinator will work in a professional medical and research environment equipped for clinical trials, including phlebotomy and patient visits. The role involves regular interaction with patients, investigators, and clinical staff in a structured, protocol-driven setting. The facility is designed to support high-quality clinical research, with designated areas for patient assessments, sample collection, and documentation.

Job Type & Location

This is a Permanent position based out of Phoenix, AZ.

Pay and Benefits

The pay range for this position is $58000.00 - $68000.00/yr.

Benefits. Benefits. Benefits. Benefits. Direct Placement. Direct. Benefits.

Workplace Type

This is a fully onsite position in Phoenix,AZ.

Application Deadline

This position is anticipated to close on Aug 14, 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 actalentaccommodation@actalentservices.com for other accommodation options.

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