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Clinical Research Assistant Jobs in Rio Rancho, NM

University of New Mexico

HS Research Assistant

Albuquerque, NM · On-site

$18.75 - $25.75/hr

Research Assistants are expected to work collaboratively as part of a larger research team while maintaining strict compliance with HIPAA regulations, FDA requirements, and Good Clinical Practice ...

University of New Mexico

HS Research Assistant

Albuquerque, NM · On-site

$18.75 - $25.75/hr

Research Assistants are expected to work collaboratively as part of a larger research team while maintaining strict compliance with HIPAA regulations, FDA requirements, and Good Clinical Practice ...

IQVIA

Clinical Research Coordinator

Albuquerque, NM · On-site

$35 - $42/hr

Clinical Research Coordinator - Albuquerque, NM Work SetUp: Onsite Schedule: 24 Hours/Week (Parttime) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical ...

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How much do clinical research assistant jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical research assistant in Rio Rancho, NM is $21.49, according to ZipRecruiter salary data. Most workers in this role earn between $16.39 and $24.57 per hour, depending on experience, location, and employer.

What is a clinical research assistant?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

What does a clinical research assistant do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

What are the key skills and qualifications needed to thrive as a clinical research assistant?

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What are some common challenges clinical research assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

What is the difference between Clinical Research Assistant vs Clinical Research Coordinator?

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

Can you be a clinical research assistant with no experience?

Clinical research assistant positions often require some knowledge of medical terminology and data management, but many entry-level roles are available for candidates without prior experience. Employers may provide on-the-job training and look for strong organizational skills, attention to detail, and the ability to follow protocols. Certifications such as Good Clinical Practice (GCP) can enhance prospects for those new to the field.
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Clinical Research Assistant jobs near you
Infographic showing various Clinical Research Assistant job openings in Rio Rancho, NM as of August 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, and 8% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $44,435 per year, or $21.4 per hour.

Research Assistant III

Albuquerque, NM • On-site

The Mind Research Network
Scientific Research and Development Services • 51 - 200 employees
Learn more about The Mind Research Networkexternal

$500/wk

Full-time

Posted 12 days ago

Job description

Overview
A full-time Research Assistant III position is available in the laboratory of Dr. Jon Houck at The Mind Research Network in Albuquerque, New Mexico. The Research Assistant III will work as part of a team on several federally-funded clinical research studies, including studies of non-invasive brain stimulation for the treatment of substance use disorder and studies designed to evaluate the behavioral and physiological effects of nicotine and tobacco use in human research participants, as well as other studies as needed. This is an in-person role that will involve providing analysis, preparation and quality control of data for research studies. The RA III will perform phlebotomy, collect and record vital signs, and other procedures as necessary. They will also oversee, organize, and execute daily activities for research studies including the recruitment of study participants. They will also ensure proper compliance with Institutional Review Board (IRB) and other regulatory agencies. Finally, they will inspect and set quality assurance testing models for the analysis of raw data, data in process, and finished data.
The position's work schedule is determined by research participant availability and will involve occasional evening or weekend participant appointments, with core working hours of 9:00 a.m.-5:30 p.m. Applicants should have strong communication and interpersonal skills, excellent attention to detail including the ability to closely follow study procedures, and be able to work productively as part of a team. Must have competence with or be able to learn to work with departmental computer systems including but not limited to Microsoft Office and Google Workspace.
Qualifications
Bachelor's degree in Psychology, Neuroscience, or a related research field and 2 years or more of relevant experience; or an equivalent combination of education, training and/or experience from which comparable knowledge, skills and abilities and have been attained.
Must have a demonstrated understanding of the principals, methods and procedures of basic medical and/or clinical research as well as the ability to understand and follow basic scientific research protocols and procedures
Strong interpersonal skills and the ability to effectively communicate with a wide range of individuals. Strong written and verbal communication skills, the ability to work independently and as a part of a team. Must have working knowledge of Microsoft Office, as well as the ability to learn department-specific computer systems as needed.
Must be able to pass a background check.
The Mind Research Network is division of Lovelace dedicated to advancing the diagnosis and treatment of mental illness and brain injury.
Headquartered in Albuquerque, New Mexico, MRN consists of an interdisciplinary association of scientists located at universities, national laboratories and research centers around the world and is focused on imaging technology and its emergence as an integral element of neuroscience investigation.
Preferred/Additional Qualifications
  • A master of science degree (M.S., M.Sc.) is preferred.
  • Experience with REDCap is preferred.
  • Two years of recent experience performing in-person procedures with clinical research participants is preferred.
  • Emergency medical services certification (e.g., EMT-B) is preferred.
  • CCRP, CCRC, or similar clinical research certification is preferred. If applicant does not have a current clinical research certification, applicant must meet requirements to apply for certification upon hire, and obtain the certification (at company's cost) within a year.

Physical Requirements
Work is performed in a dry laboratory environment. Will operate standard office equipment and will frequently stand, walk, sit, perform desk-based computer tasks, use a telephone, perform repetitive motions and occasionally lift objects that weigh up to 20 pounds. May interact with research participants.
The above is intended to describe the general requirements for the position and should not be interpreted as an exhaustive statement of physical requirements. The Institute will provide reasonable accommodation to any employee with a disability who requires an accommodation to perform the essential functions of the position.
Salary
Salary is commensurate with experience + $500 sign-on bonus.
Lovelace Biomedical is an Equal Opportunity Employer

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