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Nurses Biotech Jobs in Arizona (NOW HIRING)

Infusion Nurse - PRN/Contract

Tucson, AZ · On-site

$35 - $46.25/hr

... biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research ... The Infusion Nurse performs critical trial-related procedures and makes important trial-related ...

Infusion Nurse - PRN/Contract

Tucson, AZ

$35 - $46.25/hr

... biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research ... The Infusion Nurse performs critical trial-related procedures and makes important trial-related ...

Infusion Nurse - PRN/Contract

Tucson, AZ · On-site

$35 - $46.25/hr

... biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research ... The Infusion Nurse performs critical trial-related procedures and makes important trial-related ...

Infusion Nurse - PRN/Contract

Tucson, AZ

$35 - $46.25/hr

... biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research ... The Infusion Nurse performs critical trial-related procedures and makes important trial-related ...

At least 5 years clinical experience in hospital, home health, pharmaceutical, or biotech settings; nurse educator background a plus * Bilingual in English/Spanish and prior Ambassador experience ...

At least 5 years clinical experience in hospital, home health, pharmaceutical, or biotech settings; nurse educator background a plus * Bilingual in English/Spanish and prior Ambassador experience ...

At least 5 years clinical experience in hospital, home health, pharmaceutical, or biotech settings; nurse educator background a plus * Bilingual in English/Spanish and prior Ambassador experience ...

Microbiology Tutor

Chandler, AZ · Remote

$18 - $40/hr

... biotechnology applications. * Curriculum Awareness & Adaptive Instruction: Familiar with ... support nursing, pre-medical, and biology students at introductory through advanced levels.

Microbiology Tutor

Phoenix, AZ · Remote

$18 - $40/hr

... biotechnology applications. * Curriculum Awareness & Adaptive Instruction: Familiar with ... support nursing, pre-medical, and biology students at introductory through advanced levels.

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Showing results 1-20

Nurses Biotech information

What are Nurses in Biotech?

Nurses in biotech are registered nurses who work within the biotechnology industry, often collaborating with scientists, researchers, and medical professionals to develop and implement new medical technologies, devices, or pharmaceuticals. They may be involved in clinical trials, patient education, regulatory compliance, or product development. These nurses use their clinical expertise to ensure that biotechnological advancements are safe, effective, and meet patient care standards. Their role bridges the gap between clinical practice and scientific innovation, making them valuable assets in the advancement of healthcare.

How do nurses in the biotech industry typically collaborate with research and development teams?

Nurses in the biotech sector often work closely with research and development teams to provide clinical insights, ensure patient safety, and contribute to the design and execution of clinical trials. Their healthcare expertise allows them to bridge the gap between laboratory research and patient care, ensuring that protocols are practical and ethical. Effective collaboration usually involves regular meetings, sharing feedback on study protocols, and assisting with data collection from a clinical perspective. This cross-functional teamwork is essential for translating innovative biotech solutions into real-world healthcare improvements.

What is the difference between Nurses Biotech vs Clinical Research Nurses?

AspectNurses BiotechClinical Research Nurses
CredentialsRN license, possibly biotech-specific certificationsRN license, clinical research certifications often preferred
Work EnvironmentBiotech labs, pharmaceutical companies, research facilitiesHospitals, research clinics, clinical trial sites
Employer & IndustryBiotech firms, pharmaceutical companiesResearch institutions, hospitals, CROs
Job FocusSupporting biotech product development, lab proceduresManaging clinical trials, patient care in research

While both roles require RN licensure and involve research, Nurses Biotech primarily work in biotech labs supporting product development, whereas Clinical Research Nurses focus on managing clinical trials and patient care in clinical settings. The choice depends on whether you prefer lab-based biotech work or patient-centered clinical research.

What are the key skills and qualifications needed to thrive as a Nurse in the Biotech industry, and why are they important?

To thrive as a Nurse in the Biotech industry, you need a solid nursing background with clinical expertise, a nursing degree, and active RN licensure, often complemented by knowledge of biotechnology applications. Familiarity with laboratory information management systems (LIMS), clinical trial protocols, and compliance certifications like GCP are typically required. Strong communication, attention to detail, and adaptability help nurses collaborate with interdisciplinary teams and navigate evolving biotech environments. These skills and qualifications are crucial for ensuring patient safety, supporting research integrity, and bridging clinical practice with innovative biotech solutions.
What are popular job titles related to Nurses Biotech jobs in Arizona? For Nurses Biotech jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Nurses Biotech jobs in Arizona look for? The top searched job categories for Nurses Biotech jobs in Arizona are:
What cities in Arizona are hiring for Nurses Biotech jobs? Cities in Arizona with the most Nurses Biotech job openings:
Infographic showing various Nurses Biotech job openings in Arizona as of July 2026, with employment types broken down into 78% Full Time, 11% Part Time, and 11% Contract. Highlights an 78% In-person, and 22% Remote job distribution.
Clinical Research Associate

Contractor

Posted 14 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