ZipRecruiter

Log In

1

Clinical Research Associate Jobs in Rio Rancho, NM

University of New Mexico

Nurse Navigator

Albuquerque, NM · On-site

$49.33 - $60.68/hr

... clinical research office, and provide direct patient care. The candidate will maintain point of ... Minimum Qualifications Associate's degree in Nursing; at least 3 years of experience directly ...

next page

Showing results 1-20

All JobsClinical Research Associate JobsClinical Research Associate Jobs in Rio Rancho, NM

Clinical Research Associate information

See Rio Rancho, NM salary details

$10

$37

$62

How much do clinical research associate jobs pay per hour?

As of Jun 24, 2026, the average hourly pay for clinical research associate in Rio Rancho, NM is $37.09, according to ZipRecruiter salary data. Most workers in this role earn between $26.01 and $47.50 per hour, depending on experience, location, and employer.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant education, such as a degree in life sciences or healthcare, and experience with clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like CCRP can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or training programs.

What are Clinical Research Associates?

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, and why are they important?

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 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.

What is the work of Clinical Research Associate?

A Clinical Research Associate (CRA) monitors clinical trials to ensure they are conducted according to protocols, Good Clinical Practice (GCP), and regulatory requirements. They coordinate with investigators, review trial data, conduct site visits, and ensure compliance, often using electronic data capture systems. CRAs play a key role in maintaining trial quality and integrity throughout the study process.

How much does a CRC make?

A Clinical Research Associate (CRA) in Houston typically earns between $60,000 and $85,000 annually, depending on experience, certifications, and the complexity of the clinical trials. Entry-level CRAs may start around $55,000, while experienced professionals with specialized skills can earn over $90,000. Salaries often include benefits such as health insurance and travel allowances, and the role requires knowledge of Good Clinical Practice (GCP) and clinical trial management tools.

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.

Can you be a CRA with no experience?

Becoming a Clinical Research Associate (CRA) typically requires some background in healthcare, life sciences, or related fields, but entry-level positions may be available for candidates with strong organizational skills and relevant certifications such as GCP training. Most employers prefer candidates with some related experience or education, but internships or training programs can provide a pathway for those without prior CRA experience.
More about Clinical Research Associate jobs
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 June 2026, with employment types broken down into 67% Full Time, 32% Part Time, and 1% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $77,150 per year, or $37.1 per hour.
Nurse/Clinical Research Coord

Nurse/Clinical Research Coord

University of New Mexico

Albuquerque, NM

$66K - $83K/yr

Other

Posted 2 days ago

University Of New Mexico rating

8.5

Company rating: 8.5 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

66th of 539 rated colleges and universities

Job description

The Department of Family and Community Medicine seeks to hire a Nurse/Clinical Research Coordinator. This position will provide professional services and participant care for the UNM Research Program in Psychedelic Assisted Therapies. The individual will be a lead facilitator for the Group Assisted Psilocybin Assisted Therapy (GPAT)for PTSD. There is the potential to be involved with additional psychedelic assisted therapy studies.

GPAT is an innovative study of group Psilocybin Assisted Therapy using an affinity group model including veteran/first responders, women survivors of sexual trauma, and other groups. Preferred Qualifications include training and/or experience in psychedelic assisted therapy research, group therapy, and interest in working with individuals with PTSD and addiction. The model has been created to in alignment with a community engagement process. There is the potential for the Nurse/Clinical Research Coordinator to participate in a lead role designing the therapeutic model and manual which will be in context of an FDA approved clinical trial protocol.

Duties and Responsibilities

1. Conduct facilitation in accordance with approved research protocols. Working closely with the study MD and other study staff to implement the facilitation aspects of protocol including preparatory sessions, medication administration sessions, and integration sessions. Ensure that facilitation provided adheres to the research protocol.

2. Conduct full day psychedelictherapy medication sessions lasting about 8 hours and often occurring on weekends

3. Documentation of study visits, researchquestionnairesand therapy sessions inREDCapand study folders.

4. Follow-upphone calls and emails to study participants.

5. Completion of required checklists/progress notes and other source documents

6. Evaluating study participants for suicidal or homicidal risk and documenting clinical findings and decisions. Identity patients requiring therapeutic support.

7. Adherence to required completion deadlines for required University of New Mexico trainings and offered on learning central

8. Participate in study group meetings and conference calls 

What University Of New Mexico employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply