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Clinical Research Associate Jobs in Rio Rancho, NM

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Clinical Research Associate information

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$11

$38

$65

How much do clinical research associate jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical research associate in Rio Rancho, NM is $38.92, according to ZipRecruiter salary data. Most workers in this role earn between $27.31 and $49.81 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

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

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
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What are the most commonly searched types of Clinical Research jobs in Rio Rancho, NM?

The most popular types of Clinical Research jobs in Rio Rancho, NM are:

What job categories do people searching Clinical Research Associate jobs in Rio Rancho, NM look for?

The top searched job categories for Clinical Research Associate jobs in Rio Rancho, NM are:

What cities near Rio Rancho, NM are hiring for Clinical Research Associate jobs?

Cities near Rio Rancho, NM with the most Clinical Research Associate job openings:

Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Rio Rancho, NM as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $80,461 per year, or $38.7 per hour.

Clinical Research Mgr

Albuquerque, NM

University of New Mexico
See more jobs at University of New Mexicoexternal

Full-time

Re-posted 9 days ago

University Of New Mexico rating

8.0

Company rating: 8.0 out of 10

Based on 58 frontline employees who took The Breakroom Quiz

Job description

The University of New Mexico's Centerfor Memory & Aging is seeking Project Manager and Lead Research Coordinatorfor the clinical core of the newly funded New Mexico Alzheimer's Disease ResearchCenter (NM ADRC). New Mexico is joining a group of Universities across theUnited States who focus on improving research and treatment for people withAlzheimer's Disease and related Dementias. https://hsc.unm.edu/medicine/departments/neurology/research/nmadrc/  The grant is expected to be fundedthrough at least 2029.
This position is a criticallyimportant part of the Clinical Core of the NM ADRC.  The selected will work closelywith the Clinical Core Leaders and will be the lead staff member for this core.
Main responsibilities will be inoverseeing the project coordination of the local site within the grant consortium.The selected candidate will be responsible for ensuring project milestones aremet, as well as day to day coordination of the human research project. Theproject involves longitudinal study of patients with Alzheimer's disease,including collection of MRI, cognitive, neurological, blood as well as optionalstudies, including PET, CSF and add on MRI studies. This position willsupervise research coordinators as well as community health workers who workdirectly with participants.  The project also involves overseeing the coordination/managementof the clinical data collection at outlying sites including Zuni and AcomaPueblos. The clinical core collaborates closely with many other multiple coreswithin the UNM ADRC. The position may include developing or modifying IRBdocuments for submission to the HRPO (IRB), or work closely with other stafffor these documents. Position may require occasional out of state travel tonational meetings, as well as occasional travel to the Zuni Pueblo or otherlocations within NM.
Additional responsibilities will include working as backupresearch coordinator and may include a cohort of participants for ongoingresearch studies, which includes recruiting, scheduling and screening patients,conducting assessments, ensuring protocol adherence for each specified study,and maintaining accurate records.  Dutiesalso include the collection, compilation, and management of study data andreview of patient records for past and present health issues. Weekly consensusdiagnosis meetings will be coordinated by this position in conjunction with theother core contributions.
The individual in this positionmust have strong interpersonal and communication skills and the ability to workeffectively with a wide range of people in a diverse community, particularlyolder adults with cognitive difficulties and their families. This position alsorequires a person with professional presentation and interpersonal skills. Theselected person must be adept at organization and project management. Thisemployee will work with confidential information and data, work directly withpatients, schedule and coordinate research appointments and examinations.Position may also include other clinical assessments, such as drawing andprocessing of blood samples, ECGs, vitals.

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