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Rn Biotech Jobs in Arizona (NOW HIRING)

EVERSANA

Diagnostic Specialist - West

Phoenix, AZ · Remote

BA/BS required; healthcare degree strongly preferred (MS, RN, PA, PharmD, PhD) * Minimum 7+ years of pharma/biotech experience in commercial, clinical/medical, or diagnostics * Proven success working ...

EVERSANA

Diagnostic Specialist - West

Phoenix, AZ · Remote

BA/BS required; healthcare degree strongly preferred (MS, RN, PA, PharmD, PhD) * Minimum 7+ years of pharma/biotech experience in commercial, clinical/medical, or diagnostics * Proven success working ...

Eversana

Diagnostic Specialist - West

Phoenix, AZ · Remote

BA/BS required; healthcare degree strongly preferred (MS, RN, PA, PharmD, PhD) * Minimum 7+ years of pharma/biotech experience in commercial, clinical/medical, or diagnostics * Proven success working ...

All JobsRn Biotech JobsRn Biotech Jobs in Arizona

Rn Biotech information

See Arizona salary details

$18

$41

$68

How much do rn biotech jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for rn biotech in Arizona is $41.45, according to ZipRecruiter salary data. Most workers in this role earn between $31.35 and $48.37 per hour, depending on experience, location, and employer.

What is an RN in biotech?

An RN in biotech is a registered nurse who works within the biotechnology industry, often focusing on research, clinical trials, laboratory work, or supporting the development of new medical technologies and treatments. These professionals combine their clinical nursing expertise with knowledge of biotechnology to ensure patient safety, gather and analyze data, and help implement new healthcare innovations. RNs in biotech may collaborate with scientists, engineers, and regulatory teams to advance medical research and product development. Their role is essential in bridging the gap between clinical practice and technological advancements in healthcare.

What are the key skills and qualifications needed to thrive as an RN in the biotech industry?

To thrive as an RN in the biotech industry, you need a solid clinical background, a nursing degree with RN licensure, and familiarity with research protocols or clinical trials. Experience with electronic data capture systems, laboratory information systems, and certifications like Good Clinical Practice (GCP) are often required. Strong analytical thinking, attention to detail, and effective communication help RNs collaborate with cross-functional teams and manage patient safety in research settings. These competencies ensure rigorous data collection, patient well-being, and regulatory compliance within complex biotech environments.

What are some common challenges RNs face when transitioning into the biotech industry?

RNs moving into the biotech sector often encounter challenges such as adapting to a more research-focused environment, familiarizing themselves with complex scientific protocols, and working with interdisciplinary teams that include scientists, engineers, and regulatory professionals. Unlike traditional clinical roles, biotech RNs may spend more time on protocol development, patient recruitment for clinical trials, and data management. Building knowledge in regulatory compliance and clinical research standards is essential, but many employers offer onboarding and training to help RNs bridge knowledge gaps.

What is the difference between Rn Biotech vs Laboratory Technician?

AspectRn BiotechLaboratory Technician
Required CredentialsBiotech or related degree, certification often preferredAssociate's or Bachelor's degree in science or related field
Work EnvironmentBiotech companies, research labs, pharmaceutical firmsHospitals, research labs, manufacturing facilities
Industry UsageResearch, development, clinical trialsSample analysis, testing, quality control

Both roles involve laboratory work in biotech and healthcare settings, but Rn Biotech typically requires a nursing or biotech background with a focus on clinical research, while Laboratory Technicians focus on sample testing and analysis. The roles often overlap in research environments but differ in credentials and daily responsibilities.

What are popular job titles related to Rn Biotech jobs in Arizona?

For Rn Biotech jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Rn Biotech jobs in Arizona look for?

The top searched job categories for Rn Biotech jobs in Arizona are:

What cities in Arizona are hiring for Rn Biotech jobs?

Cities in Arizona with the most Rn Biotech job openings:

Rn Biotech jobs near you
Infographic showing various Rn Biotech job openings in Arizona as of August 2026, with employment types broken down into 3% As Needed, 58% Full Time, 15% Part Time, and 24% Contract. Highlights an 99% Physical, and 1% Remote job distribution, with an average salary of $86,223 per year, or $41.5 per hour.

Clinical Research Associate

PSG Global Solutions

Tucson, AZ • On-site

Contractor

Re-posted 22 days ago

Job description

Company Description

Real Life Sciences' dedicated pharmaceutical and biotechnology division has been working with pharmaceutical companies, biotechnology organisations and professionals across both sectors since 1998 and since that time has focused on providing added-value recruitment services for companies working within development phases 1 to 4.

We work with large multinational companies, generics and biosimilar manufacturers, small niche biotech organisations, and all parts of the pharma and biotech supply chain, including R&D companies, clinical research organisations, manufacturing companies, marketing and medical communications agencies and regulatory affairs consultancies.

Real Life Sciences' success within pharma and biotech recruitment is based on our ability to understand our key markets and develop a business that is focused on supporting our customers as their challenges change and the industry evolves.

Job Description

POSITION SUMMARY:

Responsible for the conduct of clinical study activities to verify and validate new instrument platforms, assays and biomarkers developed by Ventana Medical Systems. Works closely with study managers and other CRA staff to complete all CRA functions associated with study planning, implementation, monitoring and closing study conduct in accordance with the principles of Good Clinical Practice (GCP). 

ESSENTIAL FUNCTIONS:

The following study related tasks are fundamental to this position, but they may be expanded or omitted at the discretion of the Clinical Manager to more effectively complete clinical research activities:

Site Management & Monitoring:

  • Conducts in-house monitoring, and may independently perform on-site monitoring in accordance with Roche and Ventana Standard Operating Procedures, ICH GCP guidelines and Regulations.
  • Participates in assessing study risks.
  • Communicates on behalf of the study manager with investigators and site staff.
  • Prepares study performance reports and provides input into study budgets.

Study Implementation:

  • Assists in preparation and independent execution of:
  • Study training presentations for investigators and site staff.
  • Study supply ordering and shipping. 
  • Investigational product release, labeling, accountability at study sites.
  • Site Readiness and Site Monitoring Plans.
  • Assay transfer and assay qualification activities.
  • Study records including site and trial master files.
  • Site qualification, site initiation, routine monitoring and close out visits and reports.
  • Document compilation for clinical study reports and document archive activities. 
  • Data management activities including user acceptance testing, data entry, and data verification as needed.

Departmental Roles:

  • Works within project teams to facilitate the conduct of standard study designs.
  • Participates in clinical affairs meetings and completes independent activities to support departmental functions.
  • Completes all internal training programs in a timely manner, and demonstrates professional development via independent reading, networking and training.
  • Adopts clinical practices that promote Quality First Time.
Qualifications

Formal Training/Education:

Bachelor of Science, RN, or BSN; OR equivalent combination of education and experience. 

Experience:

  • 2+ years of previous pharmaceutical or medical device clinical study coordination, clinical site monitoring, or clinical study management experience required or equivalent combination of education and experience.  
  • Prior experience with current Good Clinical Practices (cGCP) and Code of Federal Regulations (CFR) preferred. 
  • A background in biomedical/healthcare services with laboratory experience preferred.

Knowledge, Skills and Abilities:

  • Excellent skills in basic computer applications (Word, Excel, Access, PowerPoint).
  • Excellent writing and verbal communication skills.
  • Well organized and detail oriented.
  • Impeccable record keeping and filing skills.
  • Excellent time management skills.
  • Ability to give presentations and teach others. 
  • Ability to work effectively in a team, and also work independently on assigned tasks
  • Ability to complete intermittent overnight travel up to 30%.
Additional Information

Arnette Fleras Manansala

Consultant

Real Staffing Group

Direct line: 619.450.1016

ph.linkedin.com/in/arnette-manansala-478b91114

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