Clinical research coordinator [h1.location_city]
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Clinical research coordinator • scottsdale az
[last_updated.last_updated_variable_days]
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]
Job Title : Clinical Coordinator FLSA : Exempt.Reports To : Clinical Program Director Status : Full-time.Company Summary : Crossroads is an Arizona Department of Health Services licensed substance abuse...[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]
Celerion is committed to swift, exceptional clinical research through translational medicine.Every day, we use our experience, agility, and innovative research strategies to help get drugs to marke...[show_more][last_updated.last_updated_variable_days]
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]
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_variable_days]
A company is looking for a Clinical Research Administrative Coordinator (Remote).Key Responsibilities Manage organization and timely filing of emails in Microsoft Outlook and alert relevant team ...[show_more][last_updated.last_updated_variable_days]
Arizona Arthritis & Rheumatology Associates, P.Rheumatology practice in the United States.The practice has over 60 providers, 15 sites and over 350 employees providing assessment and treatments...[show_more][last_updated.last_updated_30]
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]
Responsibilities include but are not limited to being lead coordinator on a study, executing follow-up visits ongoing studies, query resolution and other study specific tasks.The CRC I will perform...[show_more][last_updated.last_updated_30]
Core hours 6AM-2PM Monday-Friday with flexibility needed for extended hour clinics.Community Medical Services (CMS) is hiring a Clinical Coordinator to help those suffering from addictions to opioi...[show_more][last_updated.last_updated_variable_days]
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]
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]
Relocation assistance is NOT available for this position.Candidates must currently reside within commuting distance or be able to relocate independently as well as be prepared to begin employment w...[show_more][last_updated.last_updated_variable_days]
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]
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]
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]
- [promoted]
Clinical Research Coordinator
The Insomnia and Sleep Institute of ArizonaPhoenix, AZ, US[job_card.full_time] +1
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Clinical Coordinator
Crossroads IncPhoenix, AZ, US[job_card.full_time]
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Clinical Research RN
UnavailablePhoenix, AZ, United States[job_card.full_time]
Clinical Research Pharmacist
CelerionTempe, AZ, US[job_card.full_time]
- [promoted]
Clinical Research Nurse
Arizona Arthritis & Rheumatology AssociatesPhoenix, AZ, United States[job_card.full_time]
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Clinical Research RN
CommonSpirit HealthPhoenix, AZ, United States[job_card.full_time]
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Clinical Research Coordinator
VirtualVocationsPhoenix, Arizona, United States[job_card.full_time]
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Clinical Research Coordinator
ARIZONA ARTHRITIS & RHEUMATOLOGY ASSOCIATESPhoenix, AZ, US[job_card.full_time]
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Clinical Research Coordinator
DocTrialsPhoenix, AZ, US[job_card.full_time]
Clinical Research Coordinator
Phoenix Children’sPhoenix[job_card.full_time]
Clinical Research Coordinator
SGSPhoenix, AZ, US[job_card.full_time]
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Community Medical ServicesMesa, Arizona, USA[job_card.full_time]
Clinical Research Coordinator
Phoenix Children'sPhoenix, Arizona[job_card.full_time]
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
MEDPACEPhoenix, AZ, United States[filters.remote]
[job_card.full_time]
Research Coordinator - Clinical-Only Local Candidates
Ironwood Cancer & Research CentersMesa, AZ, US[job_card.full_time]
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Certified Clinical Research Coordinator
Mayo ClinicScottsdale, Arizona, USA[job_card.full_time]
Clinical Research Nurse
MedixPhoenix, AZ, United States[job_card.full_time]
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Clinical Research GI
Protouch StaffingScottsdale, AZ, United States[job_card.part_time]
- [promoted]
Clinical Research RN
Dignity HealthPhoenix, 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