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Clinical Research Pre Screening Jobs in Arizona (NOW HIRING)

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 ...

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 ...

With programs like Future of Medicine , which makes advanced health screenings and research ... Participate in recruitment and pre-screening events (may be at another location) 

Participate in recruitment and pre-screening events (may be at another location) * Maintain ... Some Clinical Research experience preferred How We Work Together * Location : This is an on-site ...

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Clinical Research Pre Screening information

What is a clinical research pre screening specialist?

A Clinical Research Pre Screening specialist is responsible for evaluating potential participants to determine if they meet the basic eligibility criteria for clinical trials. They typically review medical histories, conduct initial assessments, and communicate with patients about the study requirements. This role is crucial in ensuring that only suitable candidates proceed to the next stages of the clinical trial process, which helps maintain the integrity and safety of the research. Pre screening specialists often work closely with clinical research coordinators and investigators.

What are the key skills and qualifications needed to thrive as a clinical research pre screening specialist?

To thrive as a Clinical Research Pre-Screening Specialist, you need a background in life sciences or healthcare, knowledge of research protocols, and attention to regulatory guidelines. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Strong interpersonal skills, attention to detail, and effective communication help in accurately evaluating candidates and collaborating with research teams. These skills ensure the accurate identification of eligible participants, compliance with study requirements, and smooth progression of clinical trials.

What are some common challenges faced by clinical research pre screening professionals, and how can they be addressed?

Clinical Research Pre-Screening professionals often face challenges such as accurately identifying eligible participants from large pools of applicants and ensuring strict adherence to study protocols and regulatory requirements. Managing sensitive patient data and maintaining clear communication with both clinical teams and potential participants can also be demanding. To address these challenges, it's important to stay organized, use standardized screening tools, and participate in regular training on compliance and privacy practices. Collaborating closely with research coordinators and maintaining up-to-date knowledge of study criteria can greatly improve efficiency and accuracy in pre-screening processes.

What is the difference between Clinical Research Pre Screening vs Clinical Research Coordinator?

AspectClinical Research Pre ScreeningClinical Research Coordinator
Primary RoleInitial participant eligibility assessment and screeningOversees entire study process, including recruitment, data collection, and follow-up
Required CredentialsHigh school diploma or equivalent; some roles may require clinical or research certificationsBachelor's degree in health or related field; often requires clinical research certification
Work EnvironmentScreening sites, clinics, or research facilitiesResearch sites, hospitals, clinics, or research institutions
Employer & Industry UsageUsed mainly during the participant recruitment phaseInvolved throughout the clinical trial lifecycle

While Clinical Research Pre Screening focuses on assessing participant eligibility at the start of a study, Clinical Research Coordinators manage the overall conduct of the trial, including recruitment, data collection, and compliance. Both roles are essential but differ in scope and responsibilities within the clinical research process.

What are popular job titles related to Clinical Research Pre Screening jobs in Arizona?

For Clinical Research Pre Screening jobs in Arizona, the most frequently searched job titles are:

What cities in Arizona are hiring for Clinical Research Pre Screening jobs?

Cities in Arizona with the most Clinical Research Pre Screening job openings:

Infographic showing various Clinical Research Pre Screening job openings in Arizona as of June 2026, with employment types broken down into 1% As Needed, 89% Full Time, 9% Part Time, and 1% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Clinical Research Coordinator

Actalent

Phoenix, AZ

$58K - $68K/yr

Full-time

Re-posted 4 days ago


Job description

Job Title: Clinical Research Coordinator

Job 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.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

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 31, 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 withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

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

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

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 applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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