Skip to content 
Clinical Research Assistant
About Mission Research Institute
At Mission Research Institute, we are driven by a simple but powerful mission: improving lives through innovative clinical research and compassionate patient care. Located in Gilbert, Arizona, our team partners with patients, physicians, and industry leaders to advance new treatments for some of the most common and impactful health conditions, including diabetes, obesity, cardiovascular disease, fatty liver disease, and other chronic illnesses. Our site participates in Phase Ib through Phase IV clinical trials across multiple therapeutic areas, helping bring tomorrow’s medical breakthroughs to patients today.
We believe that great research starts with great people. Team members work alongside experienced investigators, clinical research professionals, and healthcare providers in a collaborative, patient-centered environment built on integrity, teamwork, innovation, and a shared commitment to excellence.
Position Summary
The Clinical Research Assistant (CRA) plays a key role in supporting all study-related activities at our Gilbert site. Working closely with investigators, coordinators, and sponsors, the CRA ensures studies are conducted in accordance with study protocols, GCP guidelines, and regulatory requirements. This is an excellent opportunity for someone looking to launch or grow a career in clinical research within a supportive, mission-driven environment.
Key Responsibilities
- Assist in the screening, recruitment, and enrollment of study participants
- Collect and record vital signs including blood pressure, temperature, pulse oximetry, and heart rate
- Conduct patient interviews and gather medical history in accordance with study protocols
- Prepare, maintain, and organize accurate, audit-ready study documentation and case report forms (CRFs)
- Enter, verify, and manage study data in Electronic Data Capture (EDC) systems
- Ensure proper labeling, handling, storage, and shipment of biological specimens per protocol requirements
- Recognize and promptly report adverse events, protocol deviations, and safety concerns to the clinical team
- Assist with regulatory submissions and maintain compliance with IRB approvals and sponsor requirements
- Support sponsor and monitor visits, including preparation of source documents
- Coordinate participant scheduling, follow-up communications, and visit logistics
- Maintain patient confidentiality in accordance with HIPAA regulations
Qualifications
Required
- High school diploma or GED required; Bachelor’s degree in a life science, health science, or related field strongly preferred
- 2+ years of experience in a clinical, medical, or research setting (internships and volunteer experience considered)
- Strong organizational skills and meticulous attention to detail
- Excellent written and verbal communication skills
- Proficiency with Microsoft Office Suite (Word, Excel, Outlook)
- Ability to work independently and collaboratively in a fast-paced environment
Preferred
- Experience with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, REDCap)
- Knowledge of Good Clinical Practice (GCP) guidelines and ICH E6 standards
- ACRP or SOCRA certification (or willingness to obtain)
- Phlebotomy certification or experience with specimen collection
- Bilingual (English/Spanish) a plus given our diverse patient population
Physical Requirements
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this job.
- Regularly work at a desk using a computer for prolonged periods
- Perform repetitive motion with substantial movements of the wrists, hands, and/or fingers
- Regularly communicate via email, telephone, chat, and webcam (MS Teams, Zoom) to exchange accurate, timely information
- Frequently stand/walk, grasp objects, and perform light/fine manipulation of objects
- Occasionally move safely over uneven surfaces
Benefits
- Competitive compensation commensurate with experience
- Opportunity to work alongside experienced investigators and physician assistants in a collaborative environment
- Exposure to multiple therapeutic areas including cardiometabolic, respiratory, cardiovascular, and more
- Career growth and professional development support, including GCP training
- Meaningful work — helping patients access innovative treatments while advancing medical science
