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Clinical Research Associate Jobs in Rio Rancho, NM

IQVIA

Clinical Research Coordinator

Albuquerque, NM · On-site

$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 ...

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Clinical Research Associate information

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$11

$38

$65

How much do clinical research associate jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical research associate in Rio Rancho, NM is $38.92, according to ZipRecruiter salary data. Most workers in this role earn between $27.31 and $49.81 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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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?

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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 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $80,461 per year, or $38.7 per hour.

Principal Investigator (MD/DO) - Clinical Research - Albuquerque, NM Clinical Research

Albuquerque, NM • On-site

IMA Clinical Research, Inc.
Scientific Research and Development Services • 501 - 1,000 employees
Learn more about IMA Clinical Research, Inc.external

Other

Posted 8 days ago

Job description

Principal Investigator (MD/DO) – Clinical Research | Part-Time/Full-Time | Albuquerque, NM

IMA Clinical Research is seeking a board-certified MD or DO with a background in general medicine and/or metabolic specialties to join our Albuquerque, NM research team as a Principal Investigator. This is an opportunity to focus on clinical research in a collaborative, patient-centered environment without the demands of traditional clinical practice.

We are seeking a physician available on a part-time or full-time basis to provide oversight for ongoing and future clinical research studies.

What You'll Do:
  • Lead and oversee clinical trials (Phase II–IV; we do not conduct Phase I studies) while ensuring compliance with study protocols and regulatory requirements
  • Screen and evaluate study participants to determine eligibility
  • Monitor participant safety and report adverse events as required
  • Maintain accurate and timely study documentation
  • Collaborate with Sponsors, research staff, and site leadership to support successful trial execution
What You'll Bring:
  • MD or DO with an active, unrestricted medical license
  • Board certification in general medicine and/or metabolic specialties
  • Prior experience as a Principal Investigator in clinical trials preferred (Phase II–IV trial experience a plus)
  • Strong clinical judgment, attention to detail, and communication skills
Why Join Us:
  • Flexible part-time or full-time schedule
  • No nights, weekends, or on-call responsibilities
  • Research-focused role with meaningful patient impact
  • Collaborative, mission-driven team environment
The IMA Group is an affirmative Action/Equal Opportunity Employer

Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.

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