Top 12 Nephrology associate Jobs in California

Clinical Research Associate
Diality —Irvine, CA
- $120,000 - $135,000 a year
- Full-time
- Nursing
- Up to 50% travel
- Writing skills
Quick Apply
12d
Clinical Research Coordinator Associate (12-Month Fixed-Term)
Stanford University —Stanford, CA
- Full-time
- Hospital
- Inpatient
- Mid-level
8d
Clinical Assistant or Associate Professor of Medicine (Clinician Educator) Nephrology
USC —Los Angeles, CA
- $250,000 - $325,000 a year
- Full-time
- Medicine
- BC/BE
- Inpatient
Assistant, Associate, or Full Professor (Adjunct) Nephrology Research
UC San Diego —San Diego, CA
- $90,000 - $130,000 a year
- Online Application
- Medicine
- University
- Doctor of Philosophy
Clinical Assistant/Associate or Professor of Medicine (Part-Time) Nephrology
USC —Los Angeles, CA
- $137 - $150 an hour
- Part-time
- Medicine
- BC/BE
- Inpatient
Associate Director, Competitive Intelligence
Travere Therapeutics —San Diego, CA
- $150,000 - $195,000 a year
- Online Application
- 8 years
- Analysis skills
- Bachelor's degree
- Health insurance
- Paid time off
2d
Division of Nephrology (ZSFG) - Instructor, Assistant, Associate, or Full Professor
UC San Francisco Academic —San Francisco, CA
- $110,500 - $333,700 a year
- Online Application
- Medicine
- Inpatient
- Residential
Nephrology: Clinical X or Health Sciences Faculty (Assistant/Associate/Full Professor)
University of California, Davis —Sacramento, CA
- $210,900 - $553,500 a year
- Online Application
- Medicine
- Skilled nursing facility
- Internal Medicine
Assistant, Associate, or Full Professor (HS Clinical, Adjunct, In-Residence, Clinical X) Nephrology
UC San Diego —San Diego, CA
- $180,000 - $240,000 a year
- Online Application
- Medicine
- BC/BE
- Inpatient
Assistant, Associate, or Full Professor (HS Clinical, Clinical X, In-Residence, Adjunct) Glomerulonephritis Research
UC San Diego —San Diego, CA
- $150,000 - $250,000 a year
- Online Application
- Medicine
- BC/BE
- Residential

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Clinical Research Coordinator Associate (Hybrid) - Stanford School of Medicine
Stanford Vascular Surgery —Pleasanton, CA
A 2-year college degree plus 2 years of related work experience, or a bachelor’s degree in a related field, or an equivalent combination of education and…
$32 - $36 an hour
Quick Apply
8d
Clinical Research Coordinator Associate
Stanford University —Redwood City, CA
Two-year college degree and two years related work experience or a bachelor’s degree in a related field or an equivalent combination of related education and…
1d

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Clinical Research Associate

Diality
Irvine, CA

Quick Apply

Job Details

Full-time
$120,000 - $135,000 a year
12 days ago

Qualifications

Writing skills
ICH guidelines
Bachelor's degree
Clinical quality assurance standards
FDA regulations

Full Job Description

Description:

Company & Job Overview:

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating, and executing Diality clinical trials in compliance with applicable regulations (e.g., FDA, ISO 14155, ICH-GCP). This position plays a key role in supporting research projects at Diality, combing responsibilities of site management and administrative trial support to ensure smooth and efficient study operations.

As applicable, the CRA position works closely with clinical sites, internal departments (e.g., medical affairs, field service, clinical operations, clinical training and support), and external partners (Contract Research Organization, vendors) to ensure the quality and integrity of clinical data while maintaining adherence to study timelines.

Responsibilities:

Clinical Trial Administration

Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility questionnaires.
Maintain and organize the Trial Master File (TMF) and ensure all essential documents are current, complete, and audit-ready.
Track and manage trial documentation, including but not limited to site contracts, investigator agreements, financial disclosure forms, and training records.
Monitor study progress by updating trackers and preparing study status reports for internal and external stakeholders.

Site Management & Communication:

Establish, Monitor and Control tasks required tasks for site start-up activities during clinical trials.
Facilitate Communication Plan for clinical trial sites, including communications for internal Diality support teams
Act as a point of contact for clinical trial sites regarding study-related questions and issues.
Assist in managing site readiness, including regulatory and ethics submissions as needed, contract negotiations, and training.
Monitor site performance and compliance with protocols, regulations, and study timelines.
Support site readiness by ensuring all required study materials, such as investigator site files and study binders, are prepared and distributed.
Assist in scheduling and coordinating investigator meetings, site initiation visits (SIVs), and other study-related activities

Regulatory Compliance & Documentation:

As needed, assist with timely and accurate submission of regulatory documents, including IRB/EC approvals and site files.
Assist in writing and reviewing protocols, informed consent forms (ICFs), and other study-related documents.

Clinical Monitoring:

Perform remote monitoring activities such as source data verification (SDV) and data entry checks.
Assist with monitoring safety reporting, adverse events (AEs), and serious adverse events (SAEs).
Support quality assurance efforts by identifying protocol deviations and ensuring corrective actions.

Study Support:

Participate in the development of study tools, training materials, and site binders.
Assist in vendor and contract management for study-related services (e.g., laboratories, CROs).
Track study metrics, such as patient recruitment, site enrollment, and data collection timelines.

General Support:

Schedule and organize internal and external meetings, including drafting meeting agendas and minutes.
Assist in the preparation of presentations to both internal and external stakeholders as needed.
Support audit and inspection readiness by ensuring proper documentation and compliance with company SOPs and regulatory guidelines.

Collaboration & Reporting:

Collaborate with other Diality cross-functional teams, including regulatory, quality to ensure study compliance.
Support data management activities with data cleaning and resolving queries as applicable.
Prepare regular study updates, reports, and presentations for internal stakeholders.

Requirements:

Required Skills & Abilities

Attention to detail and problem-solving skills to ensure data quality and compliance
Strong organizational and time management skills.
Excellent written and verbal communication abilities.
Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
Ability to work independently and collaboratively in a fast-paced environment.

Education & Experience

Bachelor’s degree in a life science, healthcare, or related field (e.g., biology, nursing, or biomedical engineering).
5+ years of clinical research experience at a Sponsor, preferably in medical devices. A combination of other relevant experience (e.g., site level/CRO research) may also apply.
Familiarity with clinical trial regulations, including FDA, ISO 14155, and ICH-GCP.
Previous experience in a medical device company or knowledge of device-specific regulatory pathways.
Experience with managing remote monitoring activities or decentralized clinical trials.
Nephrology experience is a plus.

Travel

This role is primarily office-based with occasional travel (up to 50%) to clinical sites and meetings as needed.

Quick Apply

Refine Your Search

nephrology associate jobs in california

Clinical Research Associate

Clinical Research Coordinator Associate (12-Month Fixed-Term)

Clinical Assistant or Associate Professor of Medicine (Clinician Educator) Nephrology

Assistant, Associate, or Full Professor (Adjunct) Nephrology Research

Clinical Assistant/Associate or Professor of Medicine (Part-Time) Nephrology

Associate Director, Competitive Intelligence

Division of Nephrology (ZSFG) - Instructor, Assistant, Associate, or Full Professor

Nephrology: Clinical X or Health Sciences Faculty (Assistant/Associate/Full Professor)

Assistant, Associate, or Full Professor (HS Clinical, Adjunct, In-Residence, Clinical X) Nephrology

Assistant, Associate, or Full Professor (HS Clinical, Clinical X, In-Residence, Adjunct) Glomerulonephritis Research

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