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Clinical Research Coordinator Jobs in Rio Rancho, NM

University of New Mexico

Coord, Research

Albuquerque, NM · On-site

$19.56 - $26.58/hr

Organizes clinical in-service trainings, investigational team meetings and informational sessions to support study adherence; coordinates research equipment setup, operation, and maintenance

University of New Mexico

Coord,Research

Albuquerque, NM · On-site

$19.76 - $26.85/hr

Coord,Research Requisition ID req37506 Working Title Coord,Research Position Grade 10 Position ... This candidatewill also have a firm understanding of good clinical practices in conductingresearch ...

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How much do clinical research coordinator jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for clinical research coordinator in Rio Rancho, NM is $25.87, according to ZipRecruiter salary data. Most workers in this role earn between $21.01 and $27.98 per hour, depending on experience, location, and employer.

What is a clinical research coordinator?

A Clinical Research Coordinator (CRC) is a professional who manages and oversees clinical trials and research studies involving human participants. They are responsible for ensuring that studies are conducted according to protocol, regulatory requirements, and ethical standards. CRCs handle tasks such as recruiting participants, collecting and managing data, coordinating with research teams, and maintaining documentation. Their work is essential in advancing medical knowledge and ensuring the safety and rights of study participants.

What is a clinical research coordinator?

As a clinical research coordinator, your responsibilities and duties include overseeing research volunteers during medical trials for new drugs and medical devices. You train the volunteers and educate them about the trial and the rules they must follow. You also record data that they report and ensure they are doing the research ethically. Your job is to work with trial subjects, oversee the administration of medication or device usage, and conduct data collection accurately so that the results are as sound as possible. You must also report any unethical practices or concerns regarding trial volunteers to the doctors doing this research.

What are some common challenges faced by clinical research coordinators when managing multiple studies simultaneously?

Clinical Research Coordinators often manage several studies at once, which can present challenges in balancing timelines, documentation, and communication with various stakeholders. Keeping track of regulatory requirements, participant schedules, and data integrity for each study requires strong organizational skills and adaptability. Coordinators frequently collaborate with investigators, sponsors, and clinical staff to ensure protocol adherence and resolve issues quickly, making effective multitasking and prioritization essential to success in this role.

What are the key skills and qualifications needed to thrive as a Clinical Research Coordinator, and why are they important?

To thrive as a Clinical Research Coordinator, you need strong organizational abilities, attention to detail, and knowledge of clinical trial processes, often supported by a degree in life sciences or healthcare. Familiarity with regulatory compliance systems (such as GCP), electronic data capture (EDC) tools, and certifications like ACRP or SOCRA are typically required. Excellent communication, problem-solving, and teamwork skills enable effective coordination among investigators, sponsors, and patients. These competencies are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting the overall success of clinical research studies.

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

AspectClinical Research CoordinatorClinical Research Associate
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are commonOften requires a bachelor's or master's degree; certifications like CCRP or RAC are advantageous
Work EnvironmentWorks primarily at research sites, hospitals, or clinicsWorks mainly at sponsor offices, CROs, or monitoring sites
Employer & IndustryResearch institutions, hospitals, clinicsPharmaceutical companies, CROs, biotech firms
Job FocusManages daily study activities, patient recruitment, data collectionMonitors study progress, ensures compliance, verifies data accuracy

While both roles support clinical trials, Clinical Research Coordinators handle on-site study management and patient interactions, whereas Clinical Research Associates focus on monitoring and compliance from a remote or office setting. Understanding these differences helps in choosing the right career path or job search focus.

What qualifications do you need to be a clinical research coordinator?

A clinical research coordinator typically needs a bachelor's degree in health sciences, biology, or a related field. Relevant experience in clinical settings, strong organizational skills, and knowledge of Good Clinical Practice (GCP) guidelines are also important; some positions may require certification such as the Certified Clinical Research Coordinator (CCRC).
More about Clinical Research Coordinator 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:

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

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

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

Clinical Research Coordinator jobs near you
Infographic showing various Clinical Research Coordinator job openings in Rio Rancho, NM as of August 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 100% In-person job distribution, with an average salary of $53,813 per year, or $25.9 per hour.

Clinical Research Supervisor

University of New Mexico

Albuquerque, NM

Full-time

Re-posted 18 days ago

University Of New Mexico rating

8.3

Company rating: 8.3 out of 10

Based on 56 frontline employees who took The Breakroom Quiz

126th of 620 rated colleges and universities

Job description

The University of New Mexico's Center for Memory & Aging is seeking a Clinical Research Supervisor for the newly funded New Mexico Alzheimer's Disease Research Center (NM ADRC). While the term end is 2025, the grant is expected to be funded through at least 2029.  https://hsc.unm.edu/research/centers-programs/nmadrc/
The Center for Memory & Aging (CMA) at UNM is funded primarily from National Institute of Health (NIH) grant mechanisms, our main projects involve longitudinal study of older participants with and without cognitive problems, including collection of MRIs, cognitive, neurological, and biospecimen data. Currently all our research studies work with older adults, ages 50 and above. The Center for Memory & Aging is a growing center with a focus on research in Alzheimer's and related dementias. We have a long record of continued research funding.
The CMA is seeking a self-starter, motivated, candidate to coordinate the day-to day activities for research studies. The ideal candidate will have experience coordinating research clinical trials or participant-based research studies. Understanding and training in Human Research as well as Good Clinical Practice will be required.
The responsibilities will include recruiting and scheduling patients for ongoing research studies, ensuring protocol adherence for each study, and maintaining accurate records. Duties also include the collection, compilation, and management of study data. The individual in this position must have strong interpersonal and communication skills and the ability to work effectively with a wide range of people in a diverse community, particularly older adults with cognitive difficulties and their families. This employee will work with confidential information and data, work directly with patients and physicians, to schedule and coordinate research appointments and examinations. Position may involve sporadic travel for recruitment events, generally within the Albuquerque area.  
In addition to the above, the position may include assisting with the coordination of add on studies may include EEG, EKG, PET scan and other medical procedures which this position would help to coordinate. Interest or experience in other medical procedures would be an asset.

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