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Contract Research Associate Jobs in Arizona (NOW HIRING)

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W2 Contract - 2 years with possible extensions! Benefits include medical, dental, vision, and life ... The Research Associate II will design, execute, and interpret experiments and apply technical ...

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W2 Contract - 2 years with possible extensions! Benefits include medical, dental, vision, and life ... The Research Associate II will design, execute, and interpret experiments and apply technical ...

Research Associate II

Tucson, AZ ยท On-site

$27/hr

Aptask Global Workforce (AGW) is seeking a Research Associate II - Onsite position with a Global ... This is a 24+ month contract opportunity. This role involves conducting research, development, and ...

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Research Associate III - Assay Development (Contract W2 Role) Location: Tucson, AZ THE OPPORTUNITY * Conduct research, development, and manufacturing laboratory experimentation to support Ventana ...

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Research Associate II

Tucson, AZ ยท On-site

$34/hr

Aptask Global Workforce (AGW) is seeking a Research Associate II for an Onsite position with a ... This is a 24-month contract opportunity. This role involves conducting research, development, and ...

Research Associate II - Assay Development Location : Oro Valley, AZ Work Model : Onsite Hours ... M-F normal business hours Compensation : $27.00/hr Type : 2-year contract, Potential for extension ...

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Research Associate III - Assay Development (Contract W2 Role) Location: Tucson, AZ THE OPPORTUNITY * Conduct research, development, and manufacturing laboratory experimentation to support Ventana ...

New

Research Associate II - Assay Development Location : Oro Valley, AZ Work Model : Onsite Hours ... M-F normal business hours Compensation : $27.00/hr Type : 2-year contract, Potential for extension ...

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Contract Research Associate information

What is a contract research associate?

A Contract Research Associate (CRA) is a professional who is typically hired on a contractual basis to support and manage clinical trials or research projects. Their primary responsibilities include monitoring research sites, ensuring compliance with protocols and regulations, collecting and verifying data, and maintaining proper documentation. CRAs play a critical role in ensuring the integrity and safety of clinical studies, often working for pharmaceutical companies, contract research organizations (CROs), or academic institutions. The contract nature of the role means that assignments are usually project-based and may vary in duration and scope.

What are the key skills and qualifications needed to thrive as a contract research associate?

To thrive as a Contract Research Associate, you need a solid background in life sciences or a related field, attention to detail, and experience with clinical research processes. Familiarity with regulatory systems like FDA guidelines, Good Clinical Practice (GCP), data management tools, and electronic data capture (EDC) systems is typically required. Strong organizational skills, effective communication, and the ability to work independently or in teams help set candidates apart. These competencies ensure that clinical trials are conducted accurately, compliantly, and efficiently, supporting successful research outcomes.

What are some typical challenges faced by contract research associates when managing multiple studies simultaneously?

Contract Research Associates often juggle several clinical trials at once, which can pose challenges in time management and prioritization. Balancing the requirements of different sponsors, adhering to varying protocols, and ensuring accurate documentation for each study demand strong organizational skills. Additionally, staying up to date with regulatory changes and effective communication with site staff are crucial to avoid delays and ensure compliance. Developing efficient workflows and leveraging project management tools can help address these challenges.

What is the difference between Contract Research Associate vs Clinical Research Coordinator?

AspectContract Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP beneficialBachelor's degree in health sciences or related field; certifications like CCRP or CCRC advantageous
Work EnvironmentTypically in pharmaceutical or biotech companies, contract research organizations (CROs)Usually in hospitals, clinics, or research sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, academic medical centers, research institutions
Common Search & ComparisonYesYes

While both roles support clinical trials, a Contract Research Associate primarily works for pharmaceutical or biotech companies managing trial processes remotely or at sites, often on a contractual basis. A Clinical Research Coordinator typically works directly at research sites, coordinating patient visits and data collection. Both roles require similar credentials and certifications, but their work environments and employer types differ.

What are the most commonly searched types of Contract Research jobs in Arizona?

The most popular types of Contract Research jobs in Arizona are:

What cities in Arizona are hiring for Contract Research Associate jobs?

Cities in Arizona with the most Contract Research Associate job openings:

Infographic showing various Contract Research Associate job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Research Associate 3/Sr Research Associate (Stability testing)

Dawar Consulting

Tucson, AZ โ€ข On-site

$60 - $80/hr

Other

Medical, Dental, Vision, Retirement

Posted 6 days ago


Job description

Research Associate 3/Sr Research Associate (Stability testing)

Tucson, United States | Posted on 06/03/2026

Our client, a worldleader in biotechnology and life sciences, is looking for a"RA3/Sr RA (Stability Testing)"based out ofTucson, AZ.

Job Duration:LongTerm Contract(Possibility Of Extension)

Company Benefits: Medical, Dental,Vision, Paid Sick leave, 401K

Support research,development, and laboratory activities for diagnostic and scientific projectsthrough experimental design, bench execution, data analysis, andcross-functional collaboration.

Key Responsibilities:

  • Designand execute experimental plans to support project objectives.
  • Conductlaboratory bench experiments, make observations, analyze data, andinterpret results.
  • Preparetechnical reports, summaries, and quantitative analyses.
  • Developand optimize laboratory methods, techniques, and evaluation criteria.
  • Troubleshootexperimental issues and implement corrective actions.
  • Identifyopportunities to improve laboratory processes and workflows.
  • Participatein or lead crossโ€‘functional technical teams, including investigations andproject teams.
  • Presentexperimental procedures, findings, and project updates to teams andstakeholders.
  • Contributeto problem solving, project planning, and continuous improvementinitiatives.

Qualifications:

  • Bachelorโ€™sor Masterโ€™s degree in Biology, Molecular Biology, Biochemistry, BiomedicalSciences, or related field.
  • 4+years of post-college industry laboratory experience required.
  • Experience supporting stability studies, assay development, or diagnostic/biotech laboratory environments preferred.
  • Handsโ€‘onexperience with Immunohistochemistry (IHC) and In Situ Hybridization (ISH)is ideal.
  • Strongexperimental design, troubleshooting, data analysis, and technicalreporting skills.
  • Abilityto work independently and collaboratively in a crossโ€‘functional teamenvironment.
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