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Clinical Research Associate information

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$10

$37

$62

How much do clinical research associate jobs pay per hour?

As of Aug 21, 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.

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:

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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 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $77,150 per year, or $37.1 per hour.

Clinical Research Coordinator - Albuquerque, NM

IQVIA

Albuquerque, NM

$35 - $42/hr

Part-time

Medical, Life

Re-posted 24 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

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 research services. We collaborate with leading pharmaceutical, biotechnology, and medical device organizations to advance innovation and improve patient outcomes worldwide. Through scientific expertise, operational excellence, and cuttingedge technology, IQVIA is shaping the future of healthcare.

About the Role

IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This role is wellsuited for a detailoriented research professional who enjoys direct patient interaction, values data integrity, and is committed to highquality clinical research within diverse communities.

As a CRC, you will play a critical role in coordinating study operations, supporting patient recruitment and retention, performing studyrelated procedures, and ensuring adherence to study protocols and regulatory requirements.

Key Responsibilities

  • Coordinate and conduct clinical research activities in accordance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements

  • Perform studyrelated clinical procedures, including ECGs, vital signs, and biological sample collection

  • Conduct patient visits including screening, enrollment, education, orientation, and followup

  • Support patient recruitment efforts and community outreach, including bilingual (English/Spanish) communication

  • Prepare study materials, manage equipment setup, and support daily clinic operations

  • Accurately collect, document, and enter clinical data into electronic data capture (EDC) systems and case report forms (CRFs)

  • Request, review, and manage medical records to support study eligibility and documentation

  • Collaborate with investigators, sponsors, and monitors to address data queries and ensure study quality

  • Maintain a safe clinical environment and serve as a patient advocate throughout study participation

Qualifications

  • Bachelor's degree preferred, or an equivalent combination of education and relevant experience

  • Minimum of 1+ year of clinical research coordination experience, including prior study coordination

  • Handson experience with clinical research operations, including:

    • Data entry and query resolution in EDC systems

    • Chart prescreening and patient prescreening activities

    • Conducting and coordinating patient visits

    • Patient outreach and education via phone and facetoface communication regarding clinical trials

    • Scheduling study visits and managing visit logistics

    • Collection, processing, and shipping of laboratory samples

    • Recruitment activities and participant followup

    • Regulatory document review and maintenance

  • Working knowledge of clinical trial processes, GCP guidelines, and medical terminology

  • Experience requesting and managing medical records

  • Bilingual in English and Spanish (written and verbal) is preferred but not required

  • Strong organizational skills, attention to detail, and ability to work effectively with diverse teams and patient populations

Ready to Make an Impact?

Join IQVIA and contribute to highquality clinical research that advances science while serving diverse patient communities.
Apply today and be part of a team helping bring innovative treatments to patients.

Additional Information

  • This position is not eligible for visa sponsorship

#LI-CES #LI-DNP #LI-HCP #ONSITE

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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Hours and flexibility

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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