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Clinical Research Jobs in Rio Rancho, NM (NOW HIRING)

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Clinical Research information

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$46.4K

$101.6K

$178.8K

How much do clinical research jobs pay per year?

As of Sep 12, 2026, the average yearly pay for clinical research in Rio Rancho, NM is $101,570.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,600.00 and $115,900.00 per year, depending on experience, location, and employer.

What is clinical research?

Clinical research is a branch of healthcare science that focuses on studying human health and illness through clinical trials and observational studies. It aims to improve medical knowledge by testing new treatments, drugs, medical devices, or interventions in controlled environments. Clinical research professionals design, conduct, and monitor studies to ensure that data is accurate and that participant safety and ethical standards are maintained. The results of clinical research can lead to new therapies, improved patient care, and informed healthcare policies.

What are different clinical research jobs?

Some of the different types of clinical research jobs include clinical research associates, coordinators, data managers, clinical nurses, research scientists, and biostatisticians. There are also administrative, managerial, and recruitment positions. As a research associate, you monitor the clinical trials and the people administering them, such as clinical nurses and research coordinators who work under the direction of the principal investigator. As a biostatistician, your duties are to collect data about the study and analyze the results to determine if the medication or treatment shows statistically significant effects on participants.

What are the key skills and qualifications needed to thrive in clinical research, and why are they important?

To thrive in Clinical Research, you need a strong background in life sciences, data analysis, and regulatory compliance, often supported by a relevant degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are commonly required. Attention to detail, strong organizational skills, and effective communication make candidates stand out in this field. These skills ensure the integrity of research data, regulatory adherence, and successful collaboration among cross-functional teams.

What are some typical challenges faced by professionals in clinical research, and how can they be managed?

Clinical research professionals often face challenges such as strict regulatory compliance, tight timelines, and coordination among multidisciplinary teams. Managing large volumes of data and ensuring participant safety are also key concerns. Staying organized, maintaining open communication with team members, and keeping updated on regulatory changes can help professionals navigate these challenges effectively. It's also helpful to develop strong project management skills and to build collaborative relationships with investigators, sponsors, and regulatory bodies.

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

AspectClinical ResearchClinical Data Coordinator
Required CredentialsTypically a bachelor's degree in health sciences, life sciences, or related field; certifications like CCR or CCRA are commonOften a bachelor's degree in health or data management; certifications like CDMP or CCRC may be preferred
Work EnvironmentResearch sites, pharmaceutical companies, CROs, hospitalsClinical trial sites, hospitals, research organizations
Job FocusDesigning, managing, and overseeing clinical trialsManaging and ensuring accuracy of clinical trial data

Clinical Research involves overseeing entire clinical trials, including protocol development and compliance, while Clinical Data Coordinators focus on collecting, managing, and ensuring the quality of trial data. Both roles are essential in the clinical research process but differ in scope and responsibilities.

How do you become a clinical researcher?

To become a clinical researcher, typically a bachelor's degree in a health-related field such as biology, nursing, or medicine is required, followed by relevant experience or advanced education like a master's or PhD. Certification in clinical research, such as the Certified Clinical Research Professional (CCRP), can enhance job prospects. Strong analytical skills, knowledge of regulatory guidelines, and familiarity with research tools are also important.

Is clinical research a good career path?

Clinical research is a viable career that involves managing and conducting trials to test new medical treatments and drugs. It requires strong organizational skills, knowledge of regulatory guidelines, and often a background in healthcare or life sciences. The field offers opportunities for advancement and specialization, with roles in research coordination, data management, and regulatory affairs.

What do you do in a clinical research job?

A clinical research job involves designing, conducting, and managing studies to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this field collect and analyze data, ensure compliance with regulatory standards, and often work with clinical trial participants, using tools like electronic data capture systems. Strong attention to detail, knowledge of Good Clinical Practice (GCP), and relevant certifications are important for success.

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

A clinical research professional typically needs a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant certifications, like the Certified Clinical Research Professional (CCRP), and knowledge of Good Clinical Practice (GCP) guidelines are often required. Strong organizational skills and familiarity with clinical trial management systems are also important.
More about Clinical Research 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 jobs in Rio Rancho, NM look for?

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

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

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

Clinical Research jobs near you
Infographic showing various Clinical Research job openings in Rio Rancho, NM as of August 2026, with employment types broken down into 85% Full Time, 9% Part Time, and 6% Contract. Highlights an 93% In-person, and 7% Remote job distribution, with an average salary of $100,961 per year, or $48.5 per hour.

Clinical Research Coordinator - Albuquerque, NM

Albuquerque, NM • On-site

IQVIA, Inc.
Health Care and Social Assistance • 10K+ employees
Learn more about IQVIA, Inc.external

$35 - $42/hr

Part-time

Medical, Life

Re-posted 17 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

Job description

Clinical Research Coordinator - Albuquerque, NM
Work Set-Up: On-site
Schedule: 24 Hours/Week (Part-time)
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 cutting-edge 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 well-suited for a detail-oriented research professional who enjoys direct patient interaction, values data integrity, and is committed to high-quality clinical research within diverse communities.
As a CRC, you will play a critical role in coordinating study operations, supporting patient recruitment and retention, performing study-related 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 study-related clinical procedures, including ECGs, vital signs, and biological sample collection
  • Conduct patient visits including screening, enrollment, education, orientation, and follow-up
  • 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
  • Hands-on experience with clinical research operations, including:
    • Data entry and query resolution in EDC systems
    • Chart pre-screening and patient pre-screening activities
    • Conducting and coordinating patient visits
    • Patient outreach and education via phone and face-to-face communication regarding clinical trials
    • Scheduling study visits and managing visit logistics
    • Collection, processing, and shipping of laboratory samples
    • Recruitment activities and participant follow-up
    • 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 high-quality 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 at https://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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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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