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Home Based Clinical Research Associate Jobs in Arizona

Healthcare Degree

Clinical Research Coordinator

Tucson, AZ · On-site

$100 - $125/hr

There are even associate degree programs in clinical research such as the associate's of applied ... Students must complete courses in seven key areas, but they can select courses based on their ...

CommonSpirit Health

Clinical Research RN

Phoenix, AZ · On-site

... its home-based services and virtual care offerings. As our Clinician Research RN, you will leverage your clinical nursing expertise to critically support and execute clinical research studies ...

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Home Based Clinical Research Associate information

What is a home based clinical research associate?

A Home Based Clinical Research Associate (CRA) is a professional responsible for monitoring clinical trials and ensuring they comply with regulatory requirements, scientific protocols, and Good Clinical Practice guidelines, all while working remotely from home. They communicate with medical sites, review study documentation, and help maintain data integrity and patient safety. This role requires strong organizational and communication skills, as well as the ability to manage multiple tasks independently from a remote setting.

What are the key skills and qualifications needed to thrive as a home based clinical research associate?

To thrive as a Home Based Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory requirements (like GCP), and a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and relevant certifications such as ACRP or SOCRA are typically required. Excellent organizational skills, attention to detail, and strong verbal and written communication are vital for effective remote collaboration and documentation. These skills ensure clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards, even when working remotely.

What are some common challenges faced by home based clinical research associates and how can they be managed?

Home Based Clinical Research Associates (CRAs) often face challenges such as maintaining effective communication with site staff and sponsors, managing time efficiently, and staying organized while working remotely. To manage these, CRAs typically rely on regular virtual meetings, robust project management tools, and clear documentation practices. Building strong relationships with site teams and proactively addressing issues also helps ensure smooth study progress and data integrity. Adapting to evolving technologies and maintaining self-discipline are key for success in this remote role.

What is the difference between Home Based Clinical Research Associate vs On-Site Clinical Research Associate?

AspectHome Based Clinical Research AssociateOn-Site Clinical Research Associate
Work EnvironmentPrimarily remote, working from home and visiting sites as neededOn-site at clinical trial locations or sites
Required CredentialsTypically requires a clinical research certification, degree in health sciences, and relevant experienceSimilar credentials, often requiring clinical research certification and healthcare background
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and biotech firms for remote monitoring rolesCommon in hospitals, research centers, and on-site clinical trial sites

The main difference between a Home Based Clinical Research Associate and an On-Site Clinical Research Associate lies in their work environment. The home-based role allows remote monitoring and site visits, offering flexibility, while the on-site role involves working directly at clinical trial locations. Both roles require similar credentials and are integral to clinical research, but their daily operations and work settings differ significantly.

What cities in Arizona are hiring for Home Based Clinical Research Associate jobs?

Cities in Arizona with the most Home Based Clinical Research Associate job openings:

Home Based Clinical Research Associate jobs near you
Infographic showing various Home Based Clinical Research Associate job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 13% Part Time, and 6% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution.

Clinical Research Nurse

Phoenix, AZ • On-site

Arizona Arthritis & Rheumatology Associates
See more jobs at Arizona Arthritis & Rheumatology Associatesexternal

Per diem

Re-posted 18 days ago

Job description

Arizona Arthritis & Rheumatology Associates, P.C. is the largest private Rheumatology practice in the United States. The practice has over 60 providers, 15 sites and over 300 employees providing assessment and treatments for rheumatological, podiatric, and electromyography patients. Our providers work together to keep patients healthy, and are recognized for excellence in medicine and for being pioneers in new treatments, ably supported by our Research department.
We are an equal employment opportunity employer and will consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability.
Our vision is to provide the best Rheumatology care, anywhere and, to balance sustainable operation with the highest possible level of patient care. We are a seeking an ambitious, friendly, positive, and compassionate Clinical Research Nurse to join our Research department.
The Clinical Research Nurse (CRN) reports to the Director of Research and is responsible for managing assigned unblinded protocols in compliance with Protocol, FDA CFR, GCP and company SOPs. The CRN will work independently as primary pharmacy designee for unblinded clinical trials in Arizona. The CRN will travel to all sites as needed to prepare investigational medication for subcutaneous injections or intravenous infusions as PRN position. The CRN will also attend meetings, monitoring visits and has the opportunity to work from home when not needed on site.
Responsibilities:
  • Manages all assigned clinical trials unblinded pharmacy responsibilities
  • Travels to sites approximately 3 days per week to prepare investigational medication
  • Responsible for preparation of unblinded clinical trial medications for IV Or SC administration.
  • Performs dispensation of investigational product (IP) using web-based drug dispensation transactions
  • Ensures correct dose and medication is prepared for each subject visit
  • Perform subcutaneous administration for unblinded trials
  • Liaison between sponsor representative and unblinded site staff for rheumatology and gastroenterology clinical trials
  • Primary point person for all support needed from the unblinded team
  • Coordinates and scheduling all unblinded monitoring visits
  • Participates in monitoring visits from sponsors and ensures all concerns are addressed in a timely manner
  • Assists with training for new unblinded staff and performs ongoing training as needed
  • Remotely supports onsite unblinded medical assistants to ensure drug inventory is stored and accounted for in compliance with the clinical trial protocols
  • Responsible for the chain of custody and accurate accountability of investigational products and devices
  • Ensures uniform implementation of protocols by completing the required training documentation in a consistent, accurate and timely manner.
  • Performs all functions according to established policies (SOPS), procedures, regulatory and accreditation requirements, as well as applicable professional standards.
  • Provides all employees and research subjects with excellent service experience by consistently demonstrating professional decorum.
  • Travel out of state as necessary for Investigator Meetings and other AARACR sites
  • Perform other administrative duties as needed

Requirements
Minimum Qualifications:
  • Licensed Registered Nurse (RN) or Licensed Practical Nurse (LPN)
  • Infusion experience preferred
  • Clinical research experience preferred
  • Possess strong organizational skills
  • Maintains confidentiality of patient and study information
  • Excellent verbal and written communication skills
  • Reliable method of transportation
  • Willingness to travel up to 4 days a week and once a month 2.5 hours to Flagstaff & Tucson (paid travel time)
  • Willing and able to travel for investigator meetings

Apply