Top 41 research coordinator Jobs in phoenix az

Clinical Research Coordinator
The Insomnia and Sleep Institute of Arizona —Phoenix, AZ
- $17 - $35 an hour
- Part-time
- Patient monitoring
- Mid-level
- In-person
- Health insurance
- Dental insurance
Quick Apply
Behavioral Health Research Coordinator
LifeStance Health —Scottsdale, AZ
- $85,000 - $95,000 a year
- Full-time
- Nursing
- Addiction Medicine
- HIPAA
- Paid parental leave
- AD&D insurance
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6d
Clinical Research Coordinator
St Joseph Hospital & Medical Center —Phoenix, AZ
- $32.38 - $48.17 an hour
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide
Headlands Research —Phoenix, AZ
- $45,000 - $100,000 a year
- Bachelor's degree
- Psychology
- Communication skills
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Research Coordinator - Clinical Trials
Medical Advancement Centers of Arizona, LLC —Phoenix, AZ
- $55,000 - $80,000 a year
- Part-time
- Spanish
- Nursing
- Research
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator I
ALLIANCE CLINICAL LLC —Phoenix, AZ
- Full-time
- Vital signs
- Customer service
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Senior Program Coordinator – Dermatology
Mayo Clinic —Scottsdale, AZ
- $78,270.40 - $117,312.00 a year
- Weekends as needed
- Mid-level
- Master's degree
- High school diploma or GED
- Health savings account
- Health insurance
19h
Clinical Research Coordinator
Phoenix Children's Hospital —Phoenix, AZ
- Full-time
- Mid-level
- Children
- Pediatrics
- Health insurance
Research Regulatory Coordinator I
Arizona Liver Health —Peoria, AZ
- $60,000 - $75,000 a year
- Full-time
- Mid-level
- High school diploma or GED
- Travel
- Mileage reimbursement
- Health savings account
Clinical Research Coordinator
Emvera Health —Scottsdale, AZ
- $26 - $30 an hour
- Full-time
- Spanish
- HIPAA
- Mid-level
- Paid holidays
- Paid time off
Quick Apply
Clinical Research Coordinator
Arizona Center for Cancer Care —Phoenix, AZ
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Ability to walk for extended periods
Clinical Research Coordinator
Caris MPI, Inc. —Phoenix, AZ
- Weekends as needed
- Microsoft Excel
- Microsoft Outlook
- Customer service
Quick Apply
Clinical Data Coordinator
Imaging Endpoints —Scottsdale, AZ
- Mid-level
- Microsoft Office
- High school diploma or GED
Clinical Research Coordinator II
Helios Clinical Research —Phoenix, AZ
- Full-time
- Vital signs
- Mid-level
- Bachelor's degree
Quick Apply
Research Patient Recruitment Coordinator II / III (Peoria)
Arizona Liver Health —Peoria, AZ
- $60,000 - $85,000 a year
- Full-time
- Spanish
- HIPAA
- English
- Mileage reimbursement
- Health savings account
Clinical Research Coordinator
United Urology Group —Scottsdale, AZ
- Full-time
- Background check
- CPR Certification
- Customer service
- Dental insurance
- Tuition reimbursement
Quick Apply
Clinical Research Coordinator
Alcanza Clinical Research —Gilbert, AZ
- Full-time
- Spanish
- LVN
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
Clinical Research Coordinator
ALS —Phoenix, AZ
- Online Application
- Bachelor of Science
- Mid-level
- US work authorization
Research Coordinator - Clinical-Only Local Candidates
IRONWOOD PHYSICIANS,P.C. —Scottsdale, AZ
- Full-time
- Microsoft Outlook
- Patient monitoring
- Computer literacy
- Dental insurance
- 401(k)
Clinical Research Coordinator
DocTrials —Phoenix, AZ
- Full-time
- Patient monitoring
- Office
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply

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Clinical Research Coordinator

The Insomnia and Sleep Institute of Arizona -
Phoenix, AZ

Quick Apply

Job Details

Part-time
$17 - $35 an hour

Benefits

Health insurance
Dental insurance
Paid time off
Vision insurance
Flexible schedule

Qualifications

ICH guidelines
Clinical quality assurance standards
FDA regulations

Full Job Description

We are seeking a detail-oriented and dedicated Clinical Research Coordinator (CRC) to manage and execute clinical trials at the site level. The CRC is responsible for coordinating all aspects of assigned research protocols, ensuring compliance with the study protocol, ICH Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. This role serves as the primary liaison between the Principal Investigator (PI), the study participants, the Sponsor/CRO, and the Institutional Review Board (IRB).

Key Responsibilities

I. Subject Recruitment and Care

Screening and Enrollment: Implement patient recruitment strategies, screen potential participants for eligibility against protocol criteria, and obtain Informed Consent in compliance with regulatory and ethical standards.
Study Visits: Coordinate and conduct all required study visits and procedures (e.g., vital signs, ECGs, phlebotomy, physical assessments) according to the protocol schedule.
Safety Monitoring: Monitor subjects for Adverse Events (AEs) and Serious Adverse Events (SAEs). Report all events promptly to the PI, Sponsor, and IRB as required by protocol and regulatory guidelines.
Participant Retention: Maintain regular contact with study participants to promote adherence to the protocol and ensure high retention rates.

II. Data and Documentation Management

Source Documentation: Develop and maintain accurate, detailed, and concurrent source documents for all study-related activities, ensuring data integrity and traceability.
Data Entry: Accurately and timely enter clinical data into the Electronic Data Capture (EDC) system or case report forms (CRFs).
Query Resolution: Respond promptly and effectively to data queries generated by the Sponsor/CRO, ensuring resolution within specified timelines.
Record Keeping: Manage and maintain the Investigator Site File/Regulatory Binder, ensuring all essential regulatory documents are current, complete, and filed correctly.

III. Regulatory and Operational Compliance

Regulatory Submissions: Prepare and submit necessary documents and reports to the IRB (e.g., protocol amendments, continuing reviews, safety reports) under the direction of the PI.
Compliance: Adhere strictly to the study protocol, ICH-GCP, FDA regulations, and institutional Standard Operating Procedures (SOPs).
Investigational Product (IP): Manage the investigational product (study drug/device) inventory, accountability logs, storage, and dispensation in compliance with regulatory requirements.
Monitoring Visits: Facilitate and prepare for routine monitoring, auditing, and inspection visits by Sponsors, CROs, and regulatory agencies.

Qualifications and Requirements

Education: Bachelor’s degree in a health-related or life science field is preferred. An Associate’s degree with significant clinical research experience may be considered.
Experience: Minimum of 2-3 years of direct experience in clinical research coordination, or an equivalent combination of education and experience.
Knowledge: Proven working knowledge of the research process, clinical trial terminology, and strict adherence to ICH Good Clinical Practice (GCP) guidelines and FDA regulations.
Certifications: Current GCP Certification is required. Certification as a CCRP (Certified Clinical Research Professional) is highly desirable.

Skills and Competencies

Detail Orientation: Exceptional attention to detail and accuracy in documentation and data management.
Organizational Skills: Excellent planning, organizational, and time management abilities to handle multiple complex protocols simultaneously.
Communication: Strong interpersonal, written, and verbal communication skills for effective interaction with patients, investigators, and external monitors.
Technical Proficiency: Competence in using Electronic Data Capture (EDC) systems, electronic medical records (EMR), and Microsoft Office Suite.

Problem-Solving: Proactive and effective problem-solving skills to address challenges in recruitment, scheduling, and protocol deviations.

Job Types: Full-time, Part-time, Contract

Pay: $17.00 - $35.00 per hour

Benefits (FT only):

Dental insurance
Flexible schedule
Health insurance
Paid time off
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

research coordinator jobs in phoenix az

Clinical Research Coordinator

Behavioral Health Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide

Research Coordinator - Clinical Trials

Clinical Research Coordinator I

Senior Program Coordinator – Dermatology

Clinical Research Coordinator

Research Regulatory Coordinator I

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Data Coordinator

Clinical Research Coordinator II

Research Patient Recruitment Coordinator II / III (Peoria)

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Research Coordinator - Clinical-Only Local Candidates

Clinical Research Coordinator

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