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Assistant Clinical Research Rater Jobs in Arizona

Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ...

Clinical Trial Psych Rater - Hungarian Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ...

Clinical Trial Psych Rater - Hungarian Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ...

Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ...

Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ...

Clinical Trial Psych Rater

Mesa, AZ · Remote

$62K - $156K/yr

Clinical Trial Psych Rater - US Spanish Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ...

Clinical Trial Psych Rater - US Spanish Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ...

Clinical Trial Psych Rater

Gilbert, AZ · Remote

$62K - $156K/yr

Clinical Trial Psych Rater - US Spanish Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ...

Showing results 41-60

Assistant Clinical Research Rater information

What is the difference between Assistant Clinical Research Rater vs Clinical Research Coordinator?

AspectAssistant Clinical Research RaterClinical Research Coordinator
Required CredentialsHigh school diploma or equivalent; some roles may require a bachelor's degreeBachelor's degree in health sciences or related field; certification often preferred
Work EnvironmentRemote or in clinical settings; primarily data review and assessmentsClinical sites; managing study logistics and participant coordination
Employer & Industry UsageResearch organizations, pharmaceutical companies, universitiesHospitals, research institutions, pharmaceutical companies
Common Search & Comparison IntentUnderstanding entry-level roles in clinical researchManaging clinical trials and participant interactions

The Assistant Clinical Research Rater typically focuses on reviewing and assessing data, often working remotely, with minimal direct patient interaction. In contrast, the Clinical Research Coordinator manages the overall conduct of clinical trials, including participant recruitment and site management. Both roles are essential in clinical research but differ in responsibilities, required credentials, and work environment.

What are the most commonly searched types of Clinical Research Rater jobs in Arizona?

The most popular types of Clinical Research Rater jobs in Arizona are:

What cities in Arizona are hiring for Assistant Clinical Research Rater jobs?

Cities in Arizona with the most Assistant Clinical Research Rater job openings:

Clinical Research Coordinator I

ALLIANCE CLINICAL LLC

Phoenix, AZ • On-site

$24 - $32/hr

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 17 days ago


Job description

Job Description
Job Description

About the Role:

The Clinical Research Coordinator supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. This role involves direct interaction with participants and plays a key part in maintaining study integrity and quality.

Duties and Responsibilities:

  • Communicate clearly and professionally with study participants regarding study objectives and ongoing instructions.
  • Administer questionnaires and monitor participant compliance with study protocols.
  • Respond to participant needs promptly and appropriately.
  • Collect and document patient medical history and health conditions.
  • Obtain and document informed consent from study participants.
  • Maintain accurate records of study drug dispensation and accountability.
  • Coordinate with laboratories to ensure timely testing and reporting.
  • Collect and assess information on concomitant medications.
  • Review and evaluate medical records for protocol compliance.
  • Perform and document assessments for adverse events (AEs) and serious adverse events (SAEs).
  • Conduct clinical procedures including EKGs, vital signs, nasal swabs, and other protocol-specific tasks.
  • Review and evaluate clinical laboratory reports.
  • Maintain up-to-date regulatory files for the research site.
  • Verify the accuracy and completeness of collected data.
  • Monitor and document temperatures for investigational product (IP) storage.
  • Support recruitment and engagement of study participants as needed.
  • Develop electronic source (e-source) documents in accordance with study protocols.
  • Manage study startup documentation, training, and timelines for assigned protocols.
  • Ensure all protocol requirements and deadlines are met consistently.
  • Adhere to all company policies, procedures, and code of conduct.
  • Maintain strict confidentiality and compliance with regulatory standards.

Qualifications:

  • At least 1 year of experience with phlebotomy and EKG procedures, or a Medical Assistant certification
  • Associate’s degree in healthcare or a related field, or equivalent relevant experience
  • 2+ years of experience in a healthcare setting
  • 2+ years of experience with FDA regulations and Good Clinical Practice (GCP)
  • Demonstrated analytical reasoning skills
  • Exceptional attention to detail and strong organizational skills
  • Excellent verbal and written communication abilities
  • Proven customer service skills with both internal and external stakeholders
  • Ability to effectively manage multiple priorities in a fast-paced environment

ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H‑1B, TN, or STEM OPT training plans) are not eligible for this role.

Benefits: Medical, Dental, Vision, 401k, PTO and more!

Location: Monday – Friday / on-site / Phoenix, AZ

About the Company:

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.