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Clinical Operations Jobs in New Mexico (NOW HIRING)

Clinical Operations Manager

Albuquerque, NM ยท On-site

$80 - $100/hr

Clinical Operations ManagerEden Pharmacy ยท Albuquerque, NM (Remote / Hybrid)REPORTS TOVP of Operations & Supply ChainTYPEFull-TimeLOCATIONRemote / HybridCOMP RANGE$65,000-$110,000 base + equityWho ...

Chief Operations Officer

Albuquerque, NM ยท On-site

$200 - $250/hr

We are seeking a Chief Operations Officer to oversee all clinical operations - including donor authorization, donor management, organ recovery, logistics, and organ utilization. This role is critical ...

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Lead daily clinical operations and oversee clinical staff. * Complete client intake evaluations, assessments, diagnoses, and clinical recommendations. * Develop, review, and update individualized ...

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Clinical Operations information

See New Mexico salary details

$33.9K

$95K

$180.7K

How much do clinical operations jobs pay per year?

As of Sep 7, 2026, the average yearly pay for clinical operations in New Mexico is $95,007.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,300.00 and $110,000.00 per year, depending on experience, location, and employer.

What is clinical operations?

Clinical operations refers to the planning, management, and execution of clinical trials and research studies within the healthcare and pharmaceutical industries. Professionals in clinical operations ensure that studies are conducted efficiently, ethically, and in compliance with regulatory requirements. Their responsibilities may include site management, patient recruitment, data collection, and ensuring protocol adherence. The goal is to facilitate the safe and effective development of new medical treatments and therapies.

How does a clinical operations professional typically collaborate with cross-functional teams during a clinical trial?

Clinical Operations professionals play a central role in coordinating activities among various teams such as regulatory affairs, data management, biostatistics, and clinical research associates. They ensure that timelines are met, protocols are followed, and all departments are aligned with trial objectives. Regular meetings, clear communication, and the ability to anticipate and resolve operational challenges are essential to successful collaboration. This cross-functional teamwork helps maintain trial quality and regulatory compliance throughout the study.

What are the key skills and qualifications needed to thrive in clinical operations, and why are they important?

To thrive in Clinical Operations, you need expertise in clinical trial management, regulatory compliance, and data analysis, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and electronic data capture (EDC) platforms is essential. Strong leadership, problem-solving, and communication skills help coordinate teams and ensure project timelines are met. These skills are crucial for guaranteeing efficient, compliant, and successful clinical trial execution in a highly regulated environment.

What is the difference between Clinical Operations vs Clinical Research Associate?

AspectClinical OperationsClinical Research Associate
Required CredentialsBachelor's degree, experience in clinical trial managementBachelor's degree, often with certification in clinical research
Work EnvironmentProject management, coordinating multiple trial sitesMonitoring clinical sites, ensuring protocol compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, pharmaceutical companies
Common Search & ComparisonFocuses on trial oversight and managementFocuses on site monitoring and data verification

Clinical Operations professionals oversee the planning, coordination, and management of clinical trials, ensuring they run smoothly across multiple sites. Clinical Research Associates primarily monitor clinical trial sites, verify data accuracy, and ensure compliance with protocols. While both roles require knowledge of clinical research, Clinical Operations has a broader scope involving project management, whereas CRAs focus on site-level monitoring.

What are the most commonly searched types of Clinical Operations jobs in New Mexico?

The most popular types of Clinical Operations jobs in New Mexico are:

What are popular job titles related to Clinical Operations jobs in New Mexico?

For Clinical Operations jobs in New Mexico, the most frequently searched job titles are:

What cities in New Mexico are hiring for Clinical Operations jobs?

Cities in New Mexico with the most Clinical Operations job openings:

Infographic showing various Clinical Operations job openings in New Mexico as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $95,007 per year, or $45.7 per hour.

Clinical Operations Manager

EDEN HEALTH INTERNATIONAL INC

Albuquerque, NM โ€ข Hybrid

$65K - $110K/yr

Full-time

Re-posted 13 days ago


Key responsibilities

  • Own and maintain the centralized repository for clinical documents, including monographs, Certificates of Analysis, dosing protocols, and physician SOPs, ensuring version control and change logs.

  • Serve as the primary point of contact between medical partners, pharmacy partners, and internal teams to facilitate clinical documentation updates and cross-functional coordination.

  • Support compliance and audit readiness by preparing documentation for internal QA and external regulatory audits, and coordinate updates with Legal, Compliance, and Regulatory teams.


Job description

Clinical Operations Manager

Eden Pharmacy Albuquerque, NM (Remote / Hybrid)

REPORTS TO

VP of Operations & Supply Chain

TYPE

Full-Time

LOCATION

Remote / Hybrid

COMP RANGE

$65,000-$110,000 base + equity

Who We Are

Eden is tackling America's metabolic health crisis - 80 million Americans affected, $600 billion in annual medical costs - with safe, science-backed treatment and a goal-centric culture built on risk-taking, self-empowerment, and transparency.

About the Role

You'll be the operational anchor for all things clinical content - keeping monographs, Certificates of Analysis, dosing protocols, and prescribing guidelines accurate, centralized, and audit-ready. You'll own documentation workflows, version control, and cross-functional updates with internal teams and pharmacy partners. No pharmacist license required, but you'll need to be highly organized, clinically literate, and comfortable driving complex projects - like a new-product launch - independently in a regulated environment.

Why this role matters: Our doctors and pharmacists depend on clear, current documentation to deliver safe care. You're the operational owner of that clarity, ensuring every downstream patient touchpoint is grounded in accurate clinical data.

What You'll Own

Clinical Documentation & Systems

  • Own the centralized repository for monographs, C of A reports, dosing protocols, and physician SOPs, with version control and change logs
  • Serve as the primary point of contact between medical partners, pharmacy partners, and internal telehealth ops
  • Partner with Medical, Pharmacy, and Compliance to standardize new protocols and clinical updates

Cross-Functional Coordination & Project Management

  • Bridge Medical Ops, Pharmacy Ops, and external partners to keep clinical alignment current across Google Drive, Notion, or Airtable
  • Own recurring workflows - protocol updates, document rollouts - end to end, with minimal supervision
  • Support new-product launches from a documentation standpoint and close execution gaps before they create risk

Compliance & Audit Support

  • Prepare documentation for internal QA and external regulatory audits
  • Coordinate with Legal, Compliance, and Regulatory whenever updates are required

Success Metrics

  • Documentation Currency: 100% of active clinical documents on current version with logged history
  • Audit Readiness: full documentation package assembled within 48 hours of any request
  • Turnaround: protocol updates completed within SLA, no missed stakeholder follow-ups

What You Bring

Required

  • Bachelor's degree in a related field (Public Health, Biology, Nursing, Chemistry, Health Sciences)
  • 3-7 years in healthcare operations, clinical documentation, or pharmacy support
  • Familiarity with clinical terminology, medication protocols, and health system workflows
  • Self-starter, comfortable owning projects independently in Google Workspace, Notion, Airtable, or similar

Preferred

  • Telehealth or pharmacy-ops experience; exposure to GLP-1s, metabolic health, or compounding
  • EMR implementation experience; background in 503A/503B compounding
  • Familiarity with FDA, NABP, or medical-legal review processes

First 90 Days

  • Audit the current documentation landscape for version-control gaps and build relationships with Medical, Pharmacy, and Compliance
  • Own the centralized repository end to end and run one full audit-readiness pass with no critical gaps
  • Stand up a repeatable workflow for protocol updates and support at least one product launch

Compensation & Benefits

The expected annual base salary range for this role is $65,000-$110,000, plus equity, comprehensive health benefits, and a flexible remote/hybrid schedule. Eden benchmarks compensation to role, level, and geography, and final offers factor in experience, interview signal, and location.

Housekeeping

Eden is an equal-opportunity employer. We welcome applicants of every age, race, color, ancestry, national origin, religion, disability, sex, gender identity or expression, sexual orientation, and veteran status - we believe a more diverse team builds better products and care.

edenpharmacy.com | Eden is an equal-opportunity employer.