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Clinical Research Coordinator Jobs in Rio Rancho, NM

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Clinical Research Coordinator information

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$14

$26

$39

How much do clinical research coordinator jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for clinical research coordinator in Rio Rancho, NM is $26.98, according to ZipRecruiter salary data. Most workers in this role earn between $21.92 and $29.18 per hour, depending on experience, location, and employer.

Who makes more, CRC or CRA?

In the clinical research field, Clinical Research Associates (CRAs) generally earn higher salaries than Clinical Research Coordinators (CRCs) due to their greater responsibilities in monitoring and overseeing multiple sites. CRAs often have more experience, certifications, and may work remotely or travel frequently, which can contribute to higher compensation. However, salaries vary based on experience, location, and employer.

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 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.

Is CRA an entry level job?

A Clinical Research Coordinator (CRC) role is often considered entry level, suitable for individuals with a bachelor's degree in health sciences or related fields. However, some positions may require prior experience or certifications such as Good Clinical Practice (GCP), and responsibilities can vary depending on the organization and complexity of the clinical trials.

What do Clinical Research Coordinators do?

Clinical Research Coordinators (CRCs) manage and oversee clinical trials, ensuring protocols are followed, data is accurately collected, and regulatory requirements are met. They coordinate between investigators, participants, and regulatory bodies, often using electronic data capture systems, and typically require knowledge of Good Clinical Practice (GCP) and relevant certifications. CRCs play a vital role in the successful execution of clinical studies in healthcare settings.

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 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 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 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.

More about Clinical Research Coordinator 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 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:
Clinical Research Coordinator jobs near you
Infographic showing various Clinical Research Coordinator job openings in Rio Rancho, NM as of July 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

Southwest Womens Oncology/Optimum

Albuquerque, NM • On-site

$22.25 - $29.50/hr

Full-time

Medical, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Clinical Research Coordinator
Southwest Women's Oncology | Albuquerque, New Mexico
Why This Role Matters
Clinical trials are how medicine moves forward - and for patients facing gynecologic cancer, access to a trial can mean access to a treatment that doesn't yet exist anywhere else.
The Clinical Research Coordinator is the operational core of that work. You are the person who keeps trials running cleanly, protecting data integrity, supporting patients through the research process, ensuring regulatory compliance, and serving as the connective tissue between sponsors, investigators, and the clinical team.
At Southwest Women's Oncology, clinical research is not a side program. It is a commitment to our patients and to the future of gynecologic oncology care. We hire for attitude and aptitude above all else. Credentials matter, but who you are and how you grow matter more.
Who We Are
Southwest Women's Oncology (SWWO) is New Mexico's leading gynecologic oncology practice, delivering advanced cancer care with skill, courage, and compassion.
Optimum Human and Optimum Infusion extend that mission into performance medicine, infusion services, longevity, recovery, hormone optimization, medical weight loss, peptide therapies, hyperbaric medicine, aesthetics, and human performance.
Together, we operate as a single integrated platform committed to one mission:
To deliver new possibilities in medical care, human performance, and health by uniting passion, knowledge, and skill.
The Opportunity
This is not an entry-level support role. The Clinical Research Coordinator owns the day-to-day coordination of an active gynecologic oncology trial portfolio-working with independence, precision, and genuine ownership across study start-up, patient management, data integrity, and regulatory compliance.
You will work closely with:
  • Principal Investigators and the clinical team on protocol execution and patient care integration
  • The Clinical Research Director on study planning, sponsor relationships, and operational performance
  • Pharmaceutical sponsors, CROs, and IRBs on regulatory submissions, monitoring visits, and data resolution
  • Patients navigating active trial participation, from consent through follow-up

You will bring organizational precision, regulatory fluency, and a patient-centered approach to every study you touch.
What You'll Own
Study Coordination & Start-Up
  • Own day-to-day coordination of Phase I-III gynecologic oncology clinical trials from start-up through close-out.
  • Lead study start-up activities including regulatory document preparation, IRB submissions, and site initiation logistics.
  • Prepare and maintain study binders including regulatory files, investigator site files, and patient charts.
  • Track study timelines, visit windows, protocol-required procedures, and sponsor deliverables.

Patient Management
  • Screen patients for clinical trial eligibility under investigator supervision.
  • Coordinate patient research visits, labs, imaging, and follow-up appointments with precision and care.
  • Support the informed consent process, ensuring documentation is complete, accurate, and audit-ready.
  • Serve as a trusted, knowledgeable resource for patients navigating active trial participation.

Data Integrity & Documentation
  • Enter study data accurately and on schedule into electronic data capture (EDC) systems.
  • Maintain source documentation and ensure filing practices are consistently audit-ready.
  • Resolve data queries from sponsors and CROs with accuracy and timeliness.
  • Ensure all documentation complies with Good Clinical Practice (GCP) and applicable regulatory standards.

Regulatory & Compliance
  • Maintain current regulatory files including investigator credentials, training records, and protocol amendments.
  • Assist with adverse event reporting, protocol deviation documentation, and corrective action follow-through.
  • Support monitoring visits, sponsor audits, and regulatory inspections with organized, complete documentation.

Operational & Administrative Support
  • Manage research-related communication with sponsors, CROs, and reference laboratories.
  • Maintain research supply inventory and coordinate research billing, ensuring appropriate separation of standard-of-care and research-related charges.

What Success Looks Like
First 90 Days
  • Fully oriented to active protocols, regulatory files, and trial portfolios.
  • Independently managing patient visit coordination and data entry with accuracy and timeliness.
  • Strong working relationships established with investigators, clinical staff, and sponsor contacts.

First 6 Months
  • Full study coordination responsibilities owned across active trials.
  • Regulatory files current, audit-ready, and consistently maintained.
  • Trusted by the clinical team and patients as a reliable, knowledgeable research resource.

First Year
  • Recognized as a clinical research anchor within the SWWO team.
  • Measurable contribution to enrollment performance, data quality, and trial compliance.
  • Consistently embodying the Optimum Standard.

Who Thrives Here
We want people who bring relentless positivity, a hunger to learn, and the drive to elevate everyone around them. You will likely thrive if:
  • You take ownership rather than waiting for direction.
  • You believe details matter.
  • You enjoy solving problems and seek continuous improvement.
  • You care deeply about patients and their families.
  • You value teamwork and accountability equally.
  • You're coachable, curious, and committed to mastery.

What You Bring
Required
  • 2+ years of clinical research experience, with demonstrated ownership of trial coordination responsibilities.
  • Working knowledge of Good Clinical Practice (GCP), ICH guidelines, and FDA regulatory requirements.
  • Experience with electronic data capture (EDC) systems and regulatory file management.
  • Strong knowledge of medical terminology.
  • Proficiency with EMR systems and Microsoft Office/Google Suite.
  • Exceptional organizational skills and attention to detail; able to manage multiple active protocols simultaneously.
  • Strong interpersonal and communication skills with a compassionate, patient-centered approach.

Preferred
  • Experience in oncology or gynecologic oncology clinical research.
  • Familiarity with Phase I-III therapeutic drug trials and sponsor/CRO relationships.
  • CCRP, CCRC, or equivalent clinical research certification.

Our Culture
We act with courage and embrace accountability.
We serve with precision and hold ourselves to impeccable standards-then raise them.
We reject mediocrity and the comfort of "good enough."
We measure success not only by outcomes, but by the integrity, excellence, and humanity we bring to every interaction.
Way Better. Extraordinary by Design.
If you crave mastery, meaning, and measurable impact-welcome home.
Compensation & Benefits
  • Competitive salary
  • Health benefits
  • 401(k)
  • Paid time off
  • Professional development and continuing education support
  • Opportunity to grow within the Optimum Platform

This is a full-time, on-site position at our Albuquerque, New Mexico office.

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