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Clinical Research Coordinator Jobs in Rio Rancho, NM

IQVIA

Clinical Research Coordinator

Albuquerque, NM

$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 ...

Medix

Clinical Research Coordinator

Albuquerque, NM · On-site

$28.85 - $33.65/hr

Job Summary Our client is seeking a highly motivated Clinical Research Coordinator. The primary responsibilities include project coordination, study design and conduct, effective communication, and ...

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Clinical Research Coordinator information

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$14

$25

$37

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:

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

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 Coordinator

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.

What IQVIA employees say

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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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