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Clinical Research Coordinator Jobs in Rio Rancho, NM

... Research Coordinators to support and coordinate enrollment for clinical research studies ... This individual will be responsible for working with a diverse team of clinical investigators and ...

The Research Coordinator positionwill exist in order to support funded research projects within the departmentof Ob/Gyn. This position will assist in the coordination and administration ofdaily ...

Coord,Research

Albuquerque, NM ยท On-site

$18.81/hr

Coord,Research Requisition ID req31604 Working Title Coord,Research Position Grade 10 Position ... Employees who provide services or work in patient care or clinical areas are required to be in ...

Coord,Research

Albuquerque, NM ยท On-site

$19.76 - $26.85/hr

Coord,Research Requisition ID req37602 Working Title Coord,Research Position Grade 10 Position ... Employees who provide services or work in patient care or clinical areas are required to be in ...

Coord,Research

Albuquerque, NM ยท On-site

$19.76 - $26.85/hr

Coordinates, plans and executes study promotional activities to keep clinical staff informed about active research studies. Additional responsibilities include site investigative file maintenance ...

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Clinical Research Coordinator information

See Rio Rancho, NM salary details

$14

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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).

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:

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/DHS II - Albuquerque, NM 7.21.2026

N-Power Medicine

Albuquerque, NM โ€ข On-site

$99K - $149K/yr

Full-time

Retirement

Re-posted yesterday


Job description

About N-Power Medicine
N-Power Medicine aims to establish a new paradigm in drug development by reinventing the 'how' and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients. We are building an exceptional multi-disciplinary team with diverse expertise spanning healthcare, engineering, technology and regulatory, and with people who share our core value of Empowering Community through generosity, curiosity and humility. We are working with urgency to bring better therapies to patients faster.
Position Summary
You will be a part of the rapidly changing clinical oncology environment with the opportunity to impact the future of clinical research and improve patients' lives while growing professionally at a dynamic, fast-growing, start-up organization. As theDigital Health Specialist II (internal title), you will work at a clinical site in Albuquerque, NM.
The ideal candidate has clinical oncology research experience or research experience in a healthcare setting. You are confident in your understanding of clinical workflow, patient data systems and clinical research in an oncology setting. We are looking for individuals who are motivated and ambitious professionals who desire to positively influence and innovate upon the quality of care for patients diagnosed with cancer.
Roles and Responsibilities
  • Serve as the Company's trusted face to the clinical practice, providing clinical support while advancing research data collection.
  • Interface directly with the healthcare providers and patients.
  • Perform peer review of clinical documentation for data quality and completeness.
  • Partner with Senior DHS to address any clinic or team issues and concerns.
  • Obtain informed consent for N-Power Medicine's clinical trials.
  • Assist and participate in the site clinical trial initiation and clinical trial(s) activities as assigned.
  • Ensure adherence to study protocols, data completeness and patient consent.
  • Assist in patient recruitment strategies where appropriate.
  • Foster collaborative relationships by effectively communicating with clinical site staff, internal stakeholders, and the N-Power Medicine team by attending site specific meetings.
  • Build and maintain relationships at the clinical site, becoming part of the functional team of practitioners.
  • Ensure quality and integrity of data capture, compliance and confidentiality with N-Power Medicine's and site's policies, standard operating procedures (SOPs), and Good Clinical Practice (GCP).
  • Respond to queries regarding missing, aberrant, or potential outlier data and data verification- escalate to the health care provider as necessary for resolution.
  • Provide proactive input and user experiences for our software.
  • Additional duties and responsibilities as required.
  • Generous, curious and humble.

Qualifications
  • 3+ years of experience in oncology clinical research and/or oncology ambulatory care preferred
  • Bachelor's degree, focused in health science or related field preferred
  • Certified Clinical Research Coordinator, Associate or Professional (CCRC, CCRA or CCRP) preferred
  • Knowledge of clinical trials, study-specific operating procedures and patient consent forms
  • Strong desire to drive a paradigm change in clinical research conduct and improve patients' lives
  • Compassionate focused patient care
  • Supports and encourages other team members, contributing to a positive team environment
  • Self-starter, able to work independently, prioritize actively, seek input, and problem solve in complex and fast-evolving environments
  • Results oriented focused on delivering the goals set-forth
  • Attention to detail and strong organizational skills
  • Excellent oral/written communication and interpersonal skills
  • Critical thinking and proven problem-solving skills
  • Work hours are dependent on local Network Partner Clinics (typically M-F, 8-5pm)

Please note that state-specific background checks and screenings may be required for this role. Employment is contingent upon successfully passing all applicable screenings.
Travel Requirements
  • Daily travel between sites may be required

$99,000 - $149,000 a year
The expected salary range for this position is $99,000 and $149,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. N-Power Medicine (NPM) offers equity at hire as well as a discretionary annual bonus which may be available based on Company performance. This position is eligible for company benefits.
More About Us
We are a mission driven, well -funded, rapidly growing company, eager to attract passionate professionals offering a highly attractive compensation package with a balanced and flexible work environment, competitive industry benefits as well as a 401K plan and other great company "perks."
We are an Equal Opportunity Employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Covid-19 Policy - The Company is committed to providing and maintaining a safe workplace, and to safeguard the health and well-being of our employees, families, visitors, and the community. While vaccination remains one of the most important tools in advancing the health and safety of employees and promoting the efficiency of workplaces, we are now in a different phase of our response when these measures are no longer necessary. We currently do not have mandatory COVID-19 vaccination requirements for our employees and contractors, as the COVID-19 public health emergency has ended. However, there are certain N-Power Medicine employees and contractors who, based on their role, will be required to continue to follow our 2021 COVID-19 vaccination and other requirements as mandated by N-Power Medicine's partners they serve. We reserve the right to modify or amend our corporate policy at any time.
Applicants must be currently authorized to work in the U.S. on a full-time basis. The Company will not sponsor applicants for work visas.
If you find this opportunity compelling, we encourage you to apply today! We promptly review all applications. Highly qualified candidates will be directly contacted by a team member.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.