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Fda Biologist Jobs in Arizona (NOW HIRING)

University of Arizona

Scientific Analyst II

Tucson, AZ · On-site

... biology, big data computational science, animal models of neurodegenerative disease, drug design and synthesis, FDA regulatory and toxicology requirements and clinical trial design and conduct. This ...

Apex Systems

Quality Assurance Specialist II

Phoenix, AZ · On-site

$65 - $80/hr

... or biological science - or equivalent industry experience * Minimum 3 years' experience in a Food and Drug Administration (FDA) regulated manufacturing environment. * Minimum 1-year experience ...

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$34.5K

$83.3K

$128.6K

How much do fda biologist jobs pay per year?

As of Sep 6, 2026, the average yearly pay for fda biologist in Arizona is $83,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,400.00 and $112,800.00 per year, depending on experience, location, and employer.

What is an FDA biologist?

An FDA Biologist is a scientist who evaluates biological products, research data, and laboratory studies to ensure public health and safety. They work on regulatory reviews, inspections, and policy development related to vaccines, gene therapy, blood products, and other biologics. Their role helps ensure compliance with federal regulations and supports scientific advancements in healthcare.

What are the typical daily responsibilities of an FDA biologist?

An FDA Biologist’s daily tasks often include reviewing scientific data, conducting laboratory experiments, and preparing reports on biological product submissions. You may assess the safety and efficacy of products such as vaccines or medical devices, ensuring compliance with regulatory standards. Collaboration with interdisciplinary teams—including chemists, statisticians, and regulatory affairs specialists—is common to address scientific questions and support regulatory decision-making. The role also involves staying updated on scientific advancements and regulatory changes relevant to the field. This dynamic environment provides opportunities to contribute to public health while developing specialized expertise.

What are the key skills and qualifications needed to thrive in the FDA biologist position, and why are they important?

To thrive as an FDA Biologist, you need a degree in biology or a related scientific field, strong analytical and laboratory skills, and a solid understanding of regulatory requirements. Familiarity with laboratory instruments, scientific data analysis tools, and regulatory databases such as GLP (Good Laboratory Practice) systems is important. Attention to detail, effective communication, and strong problem-solving abilities are valuable soft skills in this role. These competencies are crucial for accurately evaluating biological data, ensuring regulatory compliance, and collaborating effectively within multidisciplinary teams at the FDA.

What are popular job titles related to Fda Biologist jobs in Arizona?

For Fda Biologist jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Fda Biologist jobs in Arizona look for?

The top searched job categories for Fda Biologist jobs in Arizona are:

Fda Biologist jobs near you
Infographic showing various Fda Biologist job openings in Arizona as of August 2026, with employment types broken down into 81% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $83,314 per year, or $40.1 per hour.

Clinical Research Coordinator

Arizona Cancer Care Center

Peoria, AZ • On-site

$24 - $32/hr

Full-time

Posted 25 days ago

Key responsibilities

  • Collaborates with research team to plan, develop, and implement clinical research activities.

  • Coordinates study visits, procedures, and participant enrollment in compliance with protocols.

  • Tracks, reports, and maintains study records, including adverse events and protocol deviations.

Job description

Job Summary
The Clinical Research Coordinator (CRC) plays a pivotal role in the execution and management of clinical trials and research studies, working closely with principal investigators, research teams, and participants. This position ensures that all processes comply with regulatory, ethical, and organizational standards while contributing directly to the advancement of medical knowledge and patient care.
Duties and responsibilities
  • Collaborates with the Clinical Program Manager and physicians to identify, develop, organize, and implement clinical research activities.
  • Partners with principal investigators and clinical staff to plan and execute research protocols in compliance with IRB, FDA, and GCP guidelines.
  • Maintains data integrity and assists in the development of databases for effective data collection and analysis.
  • Oversee proper storage and accountability of investigational products in accordance with study protocols.
  • Ensures compliance with all research policies, protocols, and participant protection standards.
  • Conducts patient recruitment, screening, consenting, and enrollment in compliance with protocol requirements and ethical standards.
  • Coordinates study visits and procedures, ensuring protocol-specific assessments are scheduled and completed on time.
  • Tracks and reports adverse events and protocol deviations per regulatory guidelines and sponsor requirements.
  • Maintains and updates study records in regulatory binders and clinical trial management systems (CTMS), if applicable.
  • Demonstrates strict confidentiality and discretion in all matters related to research studies and participants.
  • Apply privacy and safety standards related to job responsibilities and research operations.
  • Performs other duties as assigned.

Working conditions
  • Works in an office or clinical setting.
  • Exposed to moderate noise levels.
  • Emphasizes collaboration with various stakeholders.
  • Necessitates effective communication and teamwork.
  • Functions in a fast-paced environment.
  • May require flexibility in working hours.
  • Requires adherence to safety protocols and compliance with healthcare regulations.
  • Valid driver's license and reliable transportation for travel between locations.

Physical requirements
  • Must be able to lift 25 lbs.
  • Must be able to sit, stand and walk for extended periods of time
  • Must be able to bend, kneel, crawl and twist as needed
  • Must be able to see, hear, type, and speak
  • Must be able to reach and pull

Qualifications/Education Requirements
  • Minimum of 2-3 years of clinical research experience required.
  • Associate or bachelor's degree in biological science, healthcare, or related medical/scientific field preferred.
  • An equivalent combination of education and relevant experience may be considered.
  • Experience with electronic data capture systems (e.g., Redcap, Medidata Rave) preferred.
  • Ability to critically evaluate information and apply problem-solving within healthcare and research settings.
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
  • Strong command of medical terminology and effective oral and written communication skills.
  • Ability to read, write, and communicate effectively in English.

Apply