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

DM Clinical

Site Manager (2752)

Albuquerque, NM · On-site

$100K - $120K/yr

At least 4 years of clinical research coordinator experience, including 2 years of management experience at a clinical research organization. Credentials: * Certified Clinical Research Coordinator ...

DM Clinical

Site Manager (3580)

Albuquerque, NM · On-site

$100K - $120K/yr

At least 4 years of clinical research coordinator experience, including 2 years of management experience at a clinical research organization. Credentials: * Certified Clinical Research Coordinator ...

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All JobsResearch Coordinator JobsResearch Coordinator Jobs in Rio Rancho, NM

Research Coordinator information

See Rio Rancho, NM salary details

$20.2K

$75.8K

$105.8K

How much do research coordinator jobs pay per year?

As of Jun 28, 2026, the average yearly pay for research coordinator in Rio Rancho, NM is $75,784.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,400.00 and $93,600.00 per year, depending on experience, location, and employer.

Can I get a research coordinator job without a degree?

Research coordinator positions typically require at least a bachelor's degree in a related field such as health sciences, biology, or psychology. However, some entry-level roles may accept relevant experience or certifications in research methods or data management, but most employers prefer candidates with formal education and strong organizational skills.

What Is a Research Coordinator?

A research coordinator supervises the daily activities of a study and monitors the activities of the subjects and researchers. As a research coordinator, your duties revolve around making sure that the study is conducted ethically and does not violate the research guidelines of the governing board or other agency. In short, you are responsible for making sure the study has as few flaws in its methodology as possible. You are also in charge of most administrative tasks. In this role, you can work on medical, technological, psychological, or other types of research projects, but you may work on clinical research most often.

What are Research Coordinators?

Research Coordinators are professionals responsible for managing and overseeing research projects, often in academic, medical, or clinical settings. They help design studies, ensure compliance with regulations, recruit and communicate with participants, and manage data collection and documentation. Research Coordinators play a crucial role in keeping projects organized, on schedule, and in accordance with ethical and institutional guidelines. They often serve as a bridge between principal investigators, participants, and regulatory bodies.

How much do research coordinators make in the US?

Research coordinators in the US typically earn a median annual salary of around $50,000 to $65,000, depending on experience, education, and location. Salaries can vary based on the complexity of the research, certifications, and the employer's size and sector.

What are some common challenges Research Coordinators face when managing multiple studies simultaneously?

Research Coordinators often juggle several studies at once, which can present challenges such as balancing competing deadlines, ensuring compliance with regulatory requirements, and managing communication among diverse stakeholders. Staying organized with detailed documentation and proactive scheduling is essential to prevent protocol deviations. Effective collaboration with principal investigators, sponsors, and clinical staff also helps to navigate unexpected changes and maintain study integrity.

What is the difference between Research Coordinator vs Research Assistant?

AspectResearch CoordinatorResearch Assistant
Required CredentialsBachelor's degree often required; some roles prefer or require a master'sTypically an undergraduate student or recent graduate; some roles may require a bachelor's degree
Work EnvironmentLeads study activities, manages protocols, interacts with stakeholdersSupports data collection, literature review, and administrative tasks
Employer & Industry UsageUsed in clinical, academic, and industry research settingsCommonly found in academic labs and research projects

The Research Coordinator generally has more responsibilities, including managing study protocols and liaising with stakeholders, while the Research Assistant provides support with data collection and administrative tasks. Both roles are essential in research projects but differ in scope and level of responsibility.

What are the key skills and qualifications needed to thrive as a Research Coordinator, and why are they important?

To thrive as a Research Coordinator, you need strong organizational abilities, attention to detail, and a relevant bachelor's degree or higher in a scientific or health-related field. Familiarity with research compliance systems, data management tools, and Institutional Review Board (IRB) protocols is commonly required. Excellent communication, problem-solving, and multitasking skills help you manage studies and collaborate effectively with diverse teams. These skills ensure the smooth execution of research projects, regulatory compliance, and the reliability of study outcomes.

What does a research coordinator do?

A research coordinator manages and oversees clinical or scientific research studies, ensuring protocols are followed, data is accurately collected, and regulatory requirements are met. They often coordinate with researchers, participants, and institutions, and may use tools like electronic data capture systems. Strong organizational skills and knowledge of research regulations are essential for this role.

Can you be a CRA with no experience?

A Clinical Research Associate (CRA) typically requires prior experience in clinical trials or related healthcare fields, as the role involves monitoring study sites and ensuring compliance. Entry-level positions may be available for those with relevant education, such as a degree in life sciences, but most employers prefer candidates with some experience or training in clinical research methods and regulations.
More about Research Coordinator jobs
What are the most commonly searched types of Research jobs in Rio Rancho, NM? The most popular types of Research jobs in Rio Rancho, NM are:
What job categories do people searching Research Coordinator jobs in Rio Rancho, NM look for? The top searched job categories for Research Coordinator jobs in Rio Rancho, NM are:
What cities near Rio Rancho, NM are hiring for Research Coordinator jobs? Cities near Rio Rancho, NM with the most Research Coordinator job openings:
Research Coordinator jobs near you

Physician - Clinical Trials - MD/DO

Headlands Research

Albuquerque, NM

Other

Posted 12 days ago

Job description

Join Us in Improving Lives through Clinical Research

At Headlands Research, we're not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we've rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon. 

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.

The Role of a Lifetime

Are you ready to make a difference? We're seeking an experienced Principal Investigator or Sub-Investigator to help us grow a new clinical research site in the Albuquerque area. Whether you're a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We're flexible-we're open to part-time or full-time commitments with flexible schedules.

Why Join Us?

  • Flexible Schedule: Work on your terms, with a schedule that fits your life.
  • Unlimited Potential: The sky's the limit. We're open to up to 40 hours per week, allowing you to maximize your impact.
  • Dynamic Team Environment: You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you'll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.

Responsibilities:

  • Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:

  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.
  • Active and unencumbered license to practice as an MD or DO within the state of New Mexico required.
  • Must be board-certified or board-eligible.
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.

Apply