ZipRecruiter

Log In

1

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

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 ...

next page

Showing results 1-20

All JobsClinical Research JobsClinical Research Jobs in Rio Rancho, NM

Clinical Research information

See Rio Rancho, NM salary details

$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.

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.

#J-18808-Ljbffr

Apply