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Physician Assistant Sub Investigator Jobs in Rio Rancho, NM

Powerback Rehab

Physician Assistant

Albuquerque, NM · On-site

$115K - $125K/yr

Full Time Provider Opportunity Sub-Acute, Long-Term Care is a sector of healthcare exploding with ... Our physicians, nurse practitioners (NPs) and physician assistants (PAs) are supported by a ...

Geneis Healthcare

Physician Assistant

Albuquerque, NM · On-site

$115K - $125K/yr

Full Time Provider Opportunity Sub-Acute, Long-Term Care is a sector of healthcare exploding with ... Our physicians, nurse practitioners (NPs) and physician assistants (PAs) are supported by a ...

Powerback Rehab

Attending Physician

Albuquerque, NM · On-site

$200K - $300K/yr

Sub-Acute, Long-Term Care is a sector of healthcare exploding with potential and work-life balance ... Our physicians, nurse practitioners (NPs) and physician assistants (PAs) are supported by a ...

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Physician Assistant Sub Investigator information

See Rio Rancho, NM salary details

$55K

$113.1K

$167K

How much do physician assistant sub investigator jobs pay per year?

As of Sep 1, 2026, the average yearly pay for physician assistant sub investigator in Rio Rancho, NM is $113,072.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,100.00 and $127,500.00 per year, depending on experience, location, and employer.

What is a physician assistant sub investigator?

A Physician Assistant Sub Investigator is a licensed physician assistant who works as part of a clinical research team, typically under the supervision of a principal investigator. In this role, they help conduct clinical trials by performing medical assessments, collecting and managing data, ensuring protocol compliance, and monitoring patient safety. They may also assist in patient recruitment, informed consent, and reporting adverse events. Their work is critical to ensuring that clinical trials are conducted ethically and according to regulatory standards.

What are the typical responsibilities of a physician assistant sub investigator during a clinical trial?

As a Physician Assistant Sub Investigator, you will play a key role in supporting the Principal Investigator by overseeing day-to-day clinical trial operations. Your responsibilities may include performing patient assessments, collecting and documenting study data, ensuring protocol compliance, and communicating with clinical research coordinators and sponsors. You will also contribute to patient safety monitoring and help address any adverse events. This position often requires strong attention to detail, excellent documentation skills, and the ability to work collaboratively within a multidisciplinary research team.

What are the key skills and qualifications needed to thrive as a physician assistant sub investigator?

To thrive as a Physician Assistant Sub Investigator, you need a solid clinical background as a licensed PA, experience in patient assessment, and knowledge of clinical research protocols. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant clinical research certifications is often required. Strong attention to detail, effective communication, and teamwork are essential soft skills for coordinating with research teams and ensuring protocol compliance. These skills and qualifications are crucial for maintaining research integrity, participant safety, and successful study outcomes.

What is the difference between Physician Assistant Sub Investigator vs Clinical Research Coordinator?

AspectPhysician Assistant Sub InvestigatorClinical Research Coordinator
CredentialsPhysician Assistant license, medical trainingResearch experience, certification (e.g., CCRP)
Work EnvironmentClinical trial sites, hospitals, research centersResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, research institutions, hospitalsResearch organizations, hospitals, academic institutions
Primary RoleAssist in clinical trial procedures, patient assessments, data collectionCoordinate study activities, manage documentation, ensure protocol compliance

While both roles support clinical research, Physician Assistant Sub Investigators focus on patient care and clinical procedures under supervision, whereas Clinical Research Coordinators handle study logistics and documentation. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Physician Assistant Sub Investigator jobs in Rio Rancho, NM?

For Physician Assistant Sub Investigator jobs in Rio Rancho, NM, the most frequently searched job titles are:

What job categories do people searching Physician Assistant Sub Investigator jobs in Rio Rancho, NM look for?

The top searched job categories for Physician Assistant Sub Investigator jobs in Rio Rancho, NM are:

What cities near Rio Rancho, NM are hiring for Physician Assistant Sub Investigator jobs?

Cities near Rio Rancho, NM with the most Physician Assistant Sub Investigator job openings:

Physician Assistant Sub Investigator jobs near you

Physician - Clinical Trials - MD/DO

Headlands Research

Albuquerque, NM • On-site

Full-time, Part-time

Re-posted 17 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