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Fda Researcher Jobs in California (NOW HIRING)

Clera

Medical AI Researcher

San Francisco, CA · On-site

$150K - $230K/yr

As a Medical AI Researcher, you'll work directly with medical imaging companies preparing FDA submissions, owning customer engagements end-to-end: from defining evaluation questions to delivering ...

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How much do fda researcher jobs pay per year?

As of Aug 29, 2026, the average yearly pay for fda researcher in California is $111,621.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,100.00 and $152,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an FDA researcher?

To thrive as an FDA Researcher, you need a strong background in biological sciences, chemistry, or a related field, often supported by an advanced degree (MS or PhD). Familiarity with laboratory information management systems (LIMS), regulatory databases, and compliance certifications such as Good Laboratory Practice (GLP) is typically required. Critical thinking, attention to detail, and clear scientific communication are vital soft skills in this role. These competencies are essential for ensuring research integrity, regulatory compliance, and the advancement of public health.

What are some common challenges FDA researchers face when conducting regulatory studies?

FDA researchers often encounter challenges related to balancing scientific rigor with regulatory timelines. Strict protocols and documentation requirements can make study design and execution more complex, especially when coordinating with multiple stakeholders such as review teams and external partners. Additionally, researchers must stay updated on evolving regulatory guidelines and policies, which requires ongoing professional development. Effective communication and adaptability are key to overcoming these obstacles while ensuring that research supports public health objectives.

How much do FDA researchers make?

FDA researchers typically earn a median annual salary of around $70,000 to $120,000, depending on experience, education, and specific role. Entry-level positions may start lower, while senior or specialized roles can exceed this range, often requiring relevant scientific or regulatory expertise.

What does a FDA researcher do?

An FDA researcher conducts scientific studies and analyzes data related to food, drugs, medical devices, or cosmetics to ensure safety and efficacy. They often work in laboratories, review research protocols, and collaborate with regulatory teams to support approval processes and policy development.

What cities in California are hiring for Fda Researcher jobs?

Cities in California with the most Fda Researcher job openings:

Fda Researcher jobs near you
Infographic showing various Fda Researcher job openings in California as of June 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution, with an average salary of $111,621 per year, or $53.7 per hour.

PRN/Per-Diem Research Nurse (RN)

Escondido, CA

Headlands Research
Scientific Research and Development Services • 51 - 200 employees
Learn more about Headlands Researchexternal

Per diem

Re-posted 27 days ago

Job description

OVERVIEW / POSITION DESCRIPTION

The AMCR Institute is a cutting-edge research institute specializing in the execution of Phase I-IV diabetes device and biopharmaceutical trials. Eligible subjects are offered the latest treatment options carried out under the strict guidelines from the Food and Drug Administration (FDA). Research subjects (Volunteers) become the most critical link in a chain of research and testing to develop breakthrough treatments for a broad range of health problems including Type 1 and Type 2 Diabetes. At all times the safety and confidentiality are guarded with the utmost concern.

As a member of AMCR Institute, you will contribute to the development of novel therapies and supportive technology for people with diabetes and be part of the discovery of new treatments.

The Clinical Research Nurse (RN) is a licensed clinical professional working with and under the direction of the Principal Investigator, Assistant Director, Lead Research Nurse, and in close conjunction with the Clinical Project Manager on early or late phase clinical trials related to the treatment of diabetes. The Clinical Research Nurse is an integral member of the clinical trial team and assumes responsibility and accountability for the direct research care of a group of research subjects during a designated time frame. The Clinical Research Nurse is responsible for assuring compliance with the Federal and State regulations relating to research and the study protocol requirements.

MATERIALS AND EQUIPMENT DIRECTLY USED

  1. Phlebotomy and IV supplies including infusion pumps
  2. Office equipment such as personal computer, printer and copier, telephone, fax
  3. Diabetes-related medical devices (e.g. glucometer, insulin delivery devices, etc.)

INTERRELATIONSHIPS

Physicians, Nurse Practitioners, Physician Assistants, Nurses, Research Staff, Research Subjects, and Clinical Office and Administrative Staff

DUTIES AND RESPONSIBILITIES

Research / Regulatory:

  1. Contributes to data collection by adhering to "Good Documentation Practices"
  2. Documents in detail the data obtained following AMCR Institute's Standard Operating Procedure (SOP).
  3. Competently recognizes signs and symptoms of Hypoglycemia, Hyperglycemia, and Ketosis and alerts the lead coordinator and clinician.
  4. Working knowledge of research protocol to understand the science behind the study.
  5. Assists research staff in specimen processing: spinning, pipetting, and analyzing using the YSI glucose instrument.
  6. Discharge research subject upon completion of in-clinic visit following the "Glycemic Discharge Protocol for AMCR Institute".

Clinical:

  1. Conducts a centered research subject assessment focusing on safety and venous access placement.
  2. Using aseptic technique, identifies the largest accessible vein and starts intravenous placement (IV) on adults and pediatric research subjects. Number of IV lines depending on the research design. May place two (2) IV lines on the same arm and/or another line on the opposite arm. 
  3. Using aseptic technique, changes IV bags PRN and adjust infusion pumps flow rate.
  4. Employs strategies in maintaining subject's safety: monitoring heating pad temperature, awareness of blood glucose levels, phlebitis.
  5. Administers research drugs and/or medications as ordered by a clinician.
  6. Using aseptic technique, assists research staff in blood drawing using a 3-way stopcock method.
  7. Assists research staff with performing vital signs and EKG tracings.
  8. Provides the tools and necessary support to subjects in learning their diabetes management responsibilities in accordance with the protocol.
  9. Provides nursing support to staff regarding diabetes issues as needed.
  10. Organizes and prioritizes workload to effectively accomplish goals.         

Communication

  1. Communicates clearly and effectively with clinicians, nursing and research staff, and research subjects.
  2. Check-in and report with the Lead Research Coordinator and/or RN at the start and end of each shift and provide a complete outgoing report.
  3. Sign / initial / and date all documents that were worked on during shift prior to leaving.

SCHEDULE

Shift availability varies depending upon the type and number of active research protocols being executed. Shift may range from 4 to 12 hours. Some flexibility may be possible depending upon the protocol. RNs are strongly encouraged to attend monthly meetings led by the Lead Research Nurse. These meetings may include protocol and skills training, updates, and other topics as needed.

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