Clinical research associate [h1.location_city]
[job_alerts.create_a_job]
Clinical research associate • scottsdale az
[last_updated.last_updated_1_hour]
We are seeking a detail-oriented and dedicated.Clinical Research Coordinator (CRC).The CRC is responsible for coordinating all aspects of assigned research protocols, ensuring compliance with the s...[show_more][last_updated.last_updated_variable_days]
Located conveniently in the heart of Phoenix, Arizona, St.Joseph's Hospital and Medical Center is a 571-bed, not-for-profit hospital that provides a wide range of health, social and support service...[show_more][last_updated.last_updated_30]
Arizona Arthritis & Rheumatology Associates, P.Rheumatology practice in the United States.The practice has over 60 providers, 15 sites and over 300 employees providing assessment and treatments for...[show_more][last_updated.last_updated_variable_days]
St Joseph Hospital & Medical Center Phoenix, Arizona.The posted compensation range of $30.CommonSpirit in good faith believes it might pay for this particular job, based on the circumstances at the...[show_more][last_updated.last_updated_variable_days]
To be eligible for this position, you must reside in the same country where the job is located.Perform monitoring and site management work to ensure that sites are conducting the study(ies) and rep...[show_more][last_updated.last_updated_variable_days]
Pharmacist Position at Celerion.Celerion is committed to swift, exceptional clinical research through translational medicine.
Every day, we use our experience, agility, and innovative research strat...[show_more][last_updated.last_updated_1_hour]
Arizona Arthritis & Rheumatology Associates, P.Rheumatology practice in the United States.The practice has over 60 providers, 15 sites and over 300 employees providing assessment and treatments...[show_more][last_updated.last_updated_variable_days]
As a Clinical Research Coordinator, you have mastered the art of multitasking, prioritizing, and efficiency.Your acute attention to detail has all your peers asking you to proofread their work (whi...[show_more][last_updated.last_updated_30]
This position is responsible for the coordination of a variety of research projects from pre-study implementation through study closure and will work independently in the acquisition of specimens; ...[show_more][last_updated.last_updated_variable_days]
The Triage / Clinical Research Nurse plays a critical role in providing high-quality patient care.This position involves assessing, prioritizing, and managing patient needs through effective commun...[show_more][last_updated.last_updated_variable_days]
Medpace is a full-service clinical contract research organization (CRO).We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.Our mi...[show_more][last_updated.last_updated_30]
This position is responsible for the coordination of a variety of research projects from pre-study implementation through study closure and will work independently in the acquisition of specimens; ...[show_more][last_updated.last_updated_30]
Ivy Brain Tumor Center Research Nurse Clinician.The Ivy Brain Tumor Center is a non-conventional, non-profit program offering state-of-the-art clinical trials for patients with the most aggressive ...[show_more][last_updated.last_updated_1_day]
HonorHealth Shea Medical Center.Looking to be part of something more meaningful? At HonorHealth, you'll be part of a team, creating a multi-dimensional care experience for our patients.You'll have ...[show_more][last_updated.last_updated_30]
Receives direction from principal investigator supervisor or other staff involved in research protocol(s).Gives direction to and works cooperatively with other research staff.Collaborates with vari...[show_more][last_updated.last_updated_variable_days]
Job Title : Part-Time Clinical Research Gastroenterologist - (Must Own Clinic / Practice).Schedule : Part-Time (0-8 hours / week).
We are seeking a board-certified Gastroenterologist to serve as a Princip...[show_more][last_updated.last_updated_variable_days]
Job Summary and Responsibilities.The Ivy Brain Tumor Center is a non-conventional, non-profit program offering state-of-the-art clinical trials for patients with the most aggressive form of brain c...[show_more][last_updated.last_updated_variable_days]
Marcus & Millichap is the nation’s leading brokerage firm specializing in real estate investments with offices nationwide.
Marcus & Millichap offers owners and investors the nation'...[show_more][last_updated.last_updated_variable_days]
The Clinical Research Nurse plays an integral role for leading the coordination and management of the assigned protocols.
Job duties will include screening potential patients for eligibility, provid...[show_more][last_updated.last_updated_variable_days]
Clinical Research Coordinator
The Insomnia and Sleep Institute of ArizonaPhoenix, AZ, US[job_card.full_time] +1
Clinical Research RN
UnavailablePhoenix, AZ, United States[job_card.full_time]
Clinical Research Nurse
Arizona Arthritis & Rheumatology AssociatesPhoenix, AZ, United States[job_card.full_time]
Clinical Research RN
CommonSpirit HealthPhoenix, AZ, United States[job_card.full_time]
Clinical Research Associate, Sponsor Dedicated
IQVIAParadise Valley, Arizona, United States[job_card.full_time] +1
- [new]
Clinical Research Pharmacist
CelerionTempe, AZ, United States[job_card.full_time]
Clinical Research Nurse
ARIZONA ARTHRITIS & RHEUMATOLOGY ASSOCIATESPhoenix, AZ, US[job_card.full_time]
- [promoted]
Clinical Research Coordinator
DocTrialsPhoenix, AZ, US[job_card.full_time]
Clinical Research Coordinator
Phoenix Children’sPhoenix[job_card.full_time]
Triage Nurse / Clinical Research Nurse
Kelly H Roy MD PCPhoenix, AZ, US[job_card.full_time]
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
MEDPACEPhoenix, AZ, United States[filters.remote]
[job_card.full_time]
Clinical Research Coordinator
Phoenix Children'sPhoenix, Arizona[job_card.full_time]
Clinical Research RN
Arizona StaffingPhoenix, AZ, United States[job_card.full_time]
RN III Clinical Research
HonorHealthScottsdale, AZ, United States[job_card.full_time] +1
Certified Clinical Research Coordinator
Mayo ClinicScottsdale, Arizona, USA[job_card.full_time]
Clinical Research GI
Protouch StaffingScottsdale, AZ, United States[job_card.part_time]
Clinical Research RN
Dignity HealthPhoenix, AZ, United States[job_card.full_time]
Research Associate
Marcus & MillichapPhoenix, AZ, US[job_card.full_time]
Clinical Research Nurse - 249685
MedixPhoenix, AZ, United States[job_card.full_time]
Clinical Research Coordinator
The Insomnia and Sleep Institute of ArizonaPhoenix, AZ, US[job_card.variable_days_ago]
[job_preview.job_type]
- [job_card.full_time]
- [job_card.part_time]
[job_card.job_description]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. 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. 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. 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. Dental insurance Flexible schedule Health insurance Paid time off Vision insurance
Job Description
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
III. Regulatory and Operational Compliance
Qualifications and Requirements
Skills and Competencies
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) :
Work Location : In person