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Clinical Research Associate Remote Jobs in Rio Rancho, NM

Remote position in any state except, NY, CA, HI, or AK Summary This Position Is Responsible For ... Review Service Requests, Collect Clinical And Non-Clinical Data, Verify Eligibility, Determine ...

Manage inbound clinical issues from firsthand staff and patients via phone; triage appropriately ... Bachelor of Science in Nursing (BSN) or Associates of Nursing (ASN) * At least 3 years of Emergency ...

Staff Attorney - Remote

Albuquerque, NM · On-site +1

$80K - $120K/yr

Admission to the NM state bar and in good standing. * 1+ years of experience working as an Associate or similar role in a law firm. * Strong legal research and writing skills. * Excellent ...

Staff Attorney - Remote

Rio Rancho, NM · On-site +1

$80K - $120K/yr

Admission to the NM state bar and in good standing. * 1+ years of experience working as an Associate or similar role in a law firm. * Strong legal research and writing skills. * Excellent ...

This is a remote opportunity with expected travel up to 50-60%. Bi-lingual candidates are preferred ... Research prospective organizations to identify the right customer stakeholders to sell to.

This is a remote opportunity with expected travel up to 50-60%. Bi-lingual candidates are preferred ... Research prospective organizations to identify the right customer stakeholders to sell to.

Schedule & Location This is a full-time, remote position, Monday through Friday. Some evening ... Partner with Care Navigators, clinicians, and judicial points of contact for integrated care * Stay ...

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Showing results 1-20

Clinical Research Associate Remote information

See Rio Rancho, NM salary details

$33.9K

$88.7K

$135K

How much do clinical research associate remote jobs pay per year?

As of Jun 24, 2026, the average yearly pay for clinical research associate remote in Rio Rancho, NM is $88,713.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,800.00 and $120,400.00 per year, depending on experience, location, and employer.

What does a Clinical Research Associate do when working remotely?

A Clinical Research Associate (CRA) working remotely is responsible for monitoring clinical trials to ensure they comply with regulatory requirements and study protocols. They coordinate with clinical sites, review data, ensure proper documentation, and communicate findings with research teams—all from a remote location. While they may occasionally travel for on-site visits, most of their tasks, such as reviewing electronic records, participating in virtual meetings, and managing trial documentation, are performed online. Remote CRAs play a vital role in maintaining the integrity and quality of clinical studies.

What are some common challenges faced by Clinical Research Associates working remotely, and how can they be addressed?

Remote Clinical Research Associates often face challenges such as coordinating across different time zones, maintaining clear communication with site staff, and ensuring data integrity without being physically present. These challenges can be addressed by leveraging robust digital tools for project management and communication, setting clear expectations with research sites, and establishing regular virtual check-ins. Staying organized, proactive, and responsive is key to successfully managing multiple studies and fostering effective collaboration from a remote environment.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (Remote), and why are they important?

To excel as a Clinical Research Associate (Remote), you generally need a background in life sciences or a related field, experience with clinical trial processes, and knowledge of regulatory guidelines like GCP. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and relevant certifications such as ACRP or SOCRA are highly valuable. Strong organizational, communication, and problem-solving skills are essential for managing remote monitoring and collaborating with research teams. These competencies ensure data integrity, regulatory compliance, and effective coordination across geographically dispersed clinical trial sites.
What job categories do people searching Clinical Research Associate Remote jobs in Rio Rancho, NM look for? The top searched job categories for Clinical Research Associate Remote jobs in Rio Rancho, NM are:
What cities near Rio Rancho, NM are hiring for Clinical Research Associate Remote jobs? Cities near Rio Rancho, NM with the most Clinical Research Associate Remote job openings:
Infographic showing various Clinical Research Associate Remote job openings in Rio Rancho, NM as of June 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 54% Full Time, 43% Part Time, and 1% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $88,713 per year, or $42.7 per hour.
Utilization Review Nurse

Utilization Review Nurse

VIVA USA INC

Albuquerque, NM • On-site, Remote

Contractor

Posted 14 days ago


Job description

Remote position in any state except, NY, CA, HI, or AK
Job Description Summary
This Position Is Responsible For Performing Discharge Care Coordination And Review Activities For Determining Efficiency, Effectiveness And Quality Of Medical/Surgical Services And Serving As Liaison Between Providers And Medical And Network Management Divisions. Review Service Requests, Collect Clinical And Non-Clinical Data, Verify Eligibility, Determine Benefit Levels In Accordance To Contract Guidelines, Conducting Initial And Concurrent Review, Prepare Reports On Quality Of Care, Identify And Report Cases, And Provide Information Regarding Utilization Management Requirements And Operational Procedures To Members, Providers And Facilities.
Job Description
1.Determine efficiency, effectiveness and quality of medical/surgical services, including appropriateness of hospital admissions, length of stay, level of care and discharge planning.
2.Serve as liaison between providers and Medical and Network Management Divisions.
3.Review service requests by receiving incoming calls, faxes, cases queued and return recorder messages to hospitals, providers and members.
4.Determine contract eligibility and benefit coverage related to precertification and/or concurrent review requests based upon information provided by hospital personnel, members and providers.
5.Determine contract eligibility and benefit coverage related to emergent referral requests.
6.Collect clinical and non-clinical data and enter information into the medical management system.
7.Utilize Medical Review Criteria, Medical Policy guidelines and internally developed review criteria to determine medical necessity, appropriateness of setting, including length of stay and type/duration of service.
8.Identify provider contract status and provider network status including facility and physician contract status.
9.Determine network status.
10.Conduct research and obtain medical information to complete the referral/certification request.
11.Utilize all Medical Management System applications to research and/or pend the precertification and referral authorization process.
12.Pend/complete certifications and/or referral authorization requests according to established policies and procedures.
13.Refer all requests that fail clinical review criteria to physician advisor.
14.Provide verbal and written notification of referrals and preauthorization determinations according to established policies/procedures.
15.Assess all cases for quality of care and report quality care issues when identified.
16.Identify and refer cases for inclusion clinical programs.
17.Report member and provider complaints according to established policies and procedures.
18.Provide information regarding UM requirements and operational procedures to members, providers and facilities.
19.Consult with supervisor/Medical Director regarding complex or difficult cases.
20.Provide professional customer service at all times to internal and external customers.
21.Follow facility procedures including checking in with designated facility personnel.
22.Document referral and precertification information according to UM policies and procedures; include plan of care/treatment, patient condition and outcomes of care for appeals and cases failing clinical review criteria.
23.Maintain knowledge of current regulatory agency standards (TDI, AAHCC/URAC, NCQA) and adhere to regulations and corporate procedures.
24.Maintain knowledge of clinical and technological advances in medical/surgical care, including pharmacological therapy.
25.Maintain knowledge of contract interpretation and containment measures (eligibility, extended care benefits and claims processing procedures).
26.Must successfully complete the UM System Competency Verification Program and maintain competency with UM systems, regulatory agency standards, tele-servicing skills, documentation requirements, advancements in medical/surgical care including pharmacological therapy, CPT-4 and ICD-10 coding.
27.Communicate and interact effectively and professionally with co-workers, management, customers, etc.
28.Comply with HIPAA, Diversity Principles, Corporate Integrity, Compliance Program policies and other applicable corporate and departmental policies.
29.Maintain complete confidentiality of company business.
30.Maintain communication with management regarding development within areas of assigned responsibilities and perform special projects as required or requested.
Requirements: LPN and UM experience
Notes:
Remote position in any state except, NY, CA, HI, or AK
VIVA is an equal opportunity employer. All qualified applicants have an equal opportunity for placement, and all employees have an equal opportunity to develop on the job. This means that VIVA will not discriminate against any employee or qualified applicant on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status