A Clinical Research Associate is responsible for running clinical trials, usually for an organization undertaking pharmacological drug testing. Will ensure that trials adhere to good clinical practice guidelines for monitoring clinical trials.
Clinical Research Assistant I or II Medical Advancement Centers of Arizona, LLC Phoenix, AZ Job Details Full-time $50,000 - $60,000 a year 5 hours ago Benefits Health insurance Dental insurance Paid time off Vision insurance Flexible schedule Qualifications Nursing Teamwork Phlebotomy specimen handling ICH guidelines Biological sampling Productivity software Clinical quality assurance standards Associate's degree Associate Degree in Nursing Ethical review application preparation FDA regulations
Full Job Description Pay:
$50,000.00 - $60,000.00 per year Job description:
Company:
MACOA Health Location:
Phoenix, AZ Onsite Employment Type:
Full Time Compensation:
Competitive hourly or salaried rate commensurate with experience
Industry:
Clinical Research Why Join MACOA Health? At MACOA Health, you will be part of a collaborative, mission-driven team conducting clinical research that directly impacts patient health outcomes. We offer opportunities for professional growth, hands-on experience across multiple therapeutic areas, and flexible work arrangements when possible. This position is ideal for a CRC ready to expand their regulatory and operational expertise, contribute meaningfully to advancing science, and work in an environment that values accuracy, compliance, and compassion. Key Responsibilities Study Conduct & Coordination Coordinate all aspects of assigned clinical trials, from screening through study close-out. Ensure compliance with ICH-GCP, FDA, and sponsor/CRO protocols. Conduct informed consent discussions with participants, ensuring comprehension and documentation per site SOPs. Patient & Investigator Support Schedule and manage participant study visits, assessments, and follow-up. Collect and process biological samples, ECGs, and other clinical procedures as required. Maintain strong communication with investigators, participants, and study teams to support safety and adherence. Data & Documentation Enter data into electronic data capture (EDC) systems in alignment with ALCOA-C+ standards. Resolve data queries and ensure CRFs/eCRFs are accurate and complete. Maintain source documents and essential records in audit-ready condition. Regulatory Compliance Prepare, submit, and maintain regulatory documents for IRB/IEC submission, approval, and continuing review. Maintain and update the regulatory binder/eReg system, ensuring completeness and compliance with sponsor and federal requirements. Track and file safety reports, protocol amendments, updated Investigator Brochures, and informed consent forms. Ensure timely reporting of adverse events (AEs/SAEs) and protocol deviations per regulatory guidelines. Support site inspections, audits, and monitoring visits by maintaining inspection-readiness. Site Operations Collaborate with investigators, site staff, and sponsor/CRO representatives to ensure trial milestones are achieved. Assist with feasibility, pre-study site qualification, and initiation visits. Contribute to recruitment and retention strategies for diverse participant enrollment. Requirements Associate's Degree or Bachelor's degree in Life Sciences, Nursing, or related field, or equivalent clinical experience. Minimum of 1-2 years of experience as a Clinical Research Assistant or CRC . Strong understanding of ICH-GCP guidelines, FDA regulations, and clinical trial conduct. Familiarity with IRB/IEC submissions and regulatory documentation. Phlebotomy or specimen handling experience. Excellent organizational and communication skills. Proficiency with EDC, CTMS, and Microsoft Office Suite. Preferred Qualifications Bilingual in Spanish Certification as a Clinical Research Coordinator (ACRP-CCRC or
SOCRA-CCRP
). Experience across multiple therapeutic areas. Experience with eRegulatory systems.
Job Type:
Full-time Benefits:
Dental insurance Flexible schedule Health insurance Paid time off Vision insurance
Education:
Associate (Required)
Experience:
Clinical Research:
1 year (Required)
Benefits:
Flexible schedule Health insurance Paid time off Vision insurance
Work Location:
In person
Benefits:
Health insurance Paid time off Vision insurance
Work Location:
In person
Pay:
$50,000.00 - $60,000.00 per year
Benefits:
Dental insurance Health insurance Paid time off Vision insurance
