Clinical Research Coordinator Allergy Asthma & Immunology Associates Scottsdale, AZ Job Details Full-time From $25 an hour 1 hour ago Benefits Health insurance Dental insurance 401(k) Paid time off Parental leave Vision insurance 401(k) matching Life insurance Qualifications Research laboratory experience Teamwork Microsoft Excel Interpersonal skills Phlebotomy specimen handling Research project coordination Clinical laboratory experience Data integrity and documentation Attention to detail Laboratory standard operating procedures Organizational skills Clinical trial standard operating procedures Implementing research protocols Patient recruitment Patient interaction Productivity software Clinical confidentiality policies Standard operating procedures (SOPs) Medical terminology Quality data entry Full Job Description Clinical Research Coordinator Medical Research of Arizona is seeking an experienced, motivated, and detail-oriented Clinical Research Coordinator (CRC) to join our growing clinical research team. The ideal candidate will have a minimum of 1 year of clinical research experience and hands-on experience with phlebotomy, laboratory specimen processing, patient recruitment, medical terminology, and clinical trial data entry. This position is ideal for someone who enjoys working directly with patients, takes initiative, and can effectively manage multiple responsibilities in a fast-paced clinical research environment. The Clinical Research Coordinator will be responsible for overseeing patient study visits, recruitment activities, laboratory processing, data entry, and study documentation for approximately five complex clinical trials within the specialties of Allergy, Asthma & Immunology.

Position Details Job Title:

Clinical Research Coordinator Employment Type:

Full-Time Schedule:

Monday-Friday, 7:00 AM-3:00

PM Location:

Scottsdale, AZ Clinical Specialties:

Allergy, Asthma & Immunology Studies:

Approximately 5 complex clinical trials Key Responsibilities Coordinate and oversee patient study visits in accordance with study protocols, visit schedules, and site SOPs. Perform and/or assist with phlebotomy and specimen collection according to protocol requirements. Process, prepare, label, store, and ship laboratory specimens while maintaining accurate documentation and specimen accountability. Assist with patient recruitment and pre-screening, including identifying potential participants and communicating study requirements. Maintain professional and consistent communication with study participants throughout their clinical trial participation. Perform accurate and timely clinical trial data entry into EDC systems and other study-specific platforms. Review source documentation for accuracy, completeness, and consistency with protocol requirements. Maintain study-specific logs, worksheets, source documents, and other essential clinical research documentation. Assist with resolving data queries and discrepancies in a timely manner. Follow study protocols, site SOPs, ICH-GCP requirements, and applicable regulatory requirements. Communicate effectively with Principal Investigators, Sub-Investigators, sponsors, CROs, laboratory vendors, and other study personnel. Assist with preparation for and support of Site Initiation Visits, Interim Monitoring Visits, Close-Out Visits, audits, and sponsor/CRO visits. Manage multiple study-related priorities while maintaining quality, accuracy, and study timelines. Perform additional clinical research responsibilities as assigned. Required Qualifications Minimum of 1 year of clinical research experience. Previous experience as a Clinical Research Coordinator or in a similar clinical research position. Current Good Clinical Practice (GCP) certification or documented GCP training required. Phlebotomy experience required. Experience with laboratory specimen processing, handling, and shipping. Experience with patient recruitment and pre-screening. Strong understanding of medical terminology. Experience with clinical trial data entry and documentation. Strong attention to detail and organizational skills. Ability to follow detailed protocols, SOPs, and study-specific procedures. Proficiency with Microsoft Word, Excel, and PowerPoint. Strong written and verbal communication skills. Ability to work independently while also functioning effectively as part of a clinical research team. Ability to maintain confidentiality and professionalism when working with clinical trial participants and study information. Ideal Candidate We are looking for a Clinical Research Coordinator who is: Positive, professional, and patient-focused Self-motivated and dependable Demonstrates a strong work ethic Organized and highly attentive to detail Able to manage multiple clinical trials and competing priorities Comfortable working directly with patients A strong team player Willing to take initiative and take ownership of assigned responsibilities Adaptable and willing to learn new protocols, systems, and procedures Committed to maintaining high standards of patient care, data integrity, and regulatory compliance About the Position This is an excellent opportunity for a Clinical Research Coordinator who wants to expand their experience by working across multiple complex clinical trials in Allergy, Asthma & Immunology. The CRC will have an active role in patient care, study coordination, recruitment, laboratory operations, data management, and overall trial execution. The successful candidate will be expected to work collaboratively with the research team while demonstrating the ability to independently manage assigned responsibilities and maintain study timelines. If you are a hardworking, self-motivated Clinical Research Coordinator who enjoys working with patients and is looking to grow within a collaborative clinical research environment, we encourage you to apply.

Job Type:

Full-time Pay:

From $25.00 per hour

Benefits:

401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Parental leave Vision insurance

Work Location:

In person