Clinical Research Associate Jobs in California, United States

The Clinical Research Coordinator / Clinical Project Associate supports clinical trials by managing study data, drug logistics, and site documentation. They coordinate meetings, maintain supplies, and assist in quality assurance under supervision.

The Pulmonary Research Program at the Cedars-Sinai Women's Guild Lung Institute aims to understand lung disease mechanisms and translate findings to improve patient health. The Clinical Research Associate I supports noncomplex research studies by collecting data, scheduling participants, assisting with IRB submissions, and ensuring regulatory compliance.

Clinical Research Associate role at Integrated Resources, Inc. involves leading 3-4 clinical studies, ensuring data integrity, and coordinating with cross‑functional teams. Candidates should have academic CRO experience, proficiency in data management, CRF design, and familiarity with FDA regulations and EDC systems.

Structure Therapeutics is a biotech company focused on developing small molecule medicines using advanced computational and structural biology techniques. The Senior Clinical Research Associate will independently manage all clinical aspects of small to medium-sized studies, ensuring compliance with GCP, SOPs, and study protocols.

Corcept Therapeutics’ Clinical Research & Development team drives the science of cortisol modulation to treat hypercortisolism and oncology. The Senior Clinical Research Associate independently manages small‑to‑medium studies, ensuring GCP, SOP, and protocol compliance while coordinating vendors, sites, and CROs.

City of Hope's Clinical Research Associate II (CRA II) manages multiple research protocols to ensure efficiency and regulatory compliance, attending clinic as needed. Day-to-day duties include protocol management, maintaining accurate documentation, compiling and submitting data, monitoring study requirements, recruiting patients, training new staff, and collecting specimens.

The Clinical Research Associate (CRA) role sits within Resmed’s Medical Affairs team, collaborating with Sleep, Respiratory Care, SaaS, ResMed Healthcare, and Asia Growth Markets to align clinical research and market access projects with strategic priorities while maintaining global regulatory compliance. Day-to-day, the CRA supports planning, start-up, execution, monitoring, and closeout of single- and multi-site clinical studies, including site coordination, EDC monitoring and data review, stu

Integrated Resources, Inc. seeks a Clinical Research Associate to support clinical operations across multiple studies. The role involves harmonizing clinical databases, maintaining supply inventories, and coordinating site binder logistics.

Medical Devices division at Abbott focuses on innovative health solutions, including diabetes care. The Clinical Research Associate I ensures quality and integrity of clinical trial data, conducts site visits, monitors compliance, and manages study documentation.

Cancer Research Center for Health Equity at Cedars‑Sinai seeks a Clinical Research Associate II to support Dr. Judy Tan’s community‑engaged studies on LGBTQ+ health. The role independently manages participant recruitment, data entry into EDCs, and regulatory submissions while ensuring GCP and HIPAA compliance.

Clinical Research & Development at Corcept Therapeutics focuses on advancing cortisol‑modulating therapies for hypercortisolism and oncology. The Clinical Research Associate II monitors study activities, ensures GCP and SOP compliance, coordinates vendor and site management, and supports protocol and document development.

Structure Therapeutics' Clinical Development Operations team seeks a Sr. Clinical Research Associate to independently manage clinical aspects of small-to-medium studies or support large-scale studies under supervision. The role ensures compliance with GCPs, SOPs, and protocols while coordinating with cross-functional teams, vendors, sites, and CROs across study start-up, enrollment, maintenance, and closeout.

IQVIA’s Clinical Research team builds and monitors clinical trials to accelerate medical innovation. The Clinical Research Associate conducts site monitoring visits, manages regulatory submissions, and ensures protocol compliance across multiple study sites.

Intuitive Surgical's Clinical Affairs team seeks a Clinical Research Associate 3 to conduct pre-market and post-market clinical studies for medical devices, ensuring regulatory compliance. Day-to-day work includes managing site start-up, performing monitoring visits, verifying EDC data, liaising with clinical sites, and contributing to study reports and publications.

IQVIA’s Clinical Research team drives site monitoring to ensure compliance with GCP and ICH. The role conducts site visits, manages recruitment plans, and maintains Trial Master Files. Based in Overland Park, KS with additional sites in Durham, NC; Parsippany, NJ; and Carlsbad, CA, the position is on-site with a hybrid travel component.

Medical & Scientific Affairs at Abbott focuses on advancing clinical research for medical devices and diagnostics. The Clinical Research Associate II will conduct multi-center studies, perform site visits, manage device shipping, ensure compliance with GCP and regulatory standards, and support data review and trial master file readiness.

Advanced Bionics (Sonova) seeks a Senior Clinical Research Associate to lead operational execution of global medical device clinical studies from start-up through close-out, advancing innovative hearing healthcare technologies. Day-to-day, you will independently manage complex investigative sites, conduct SQV/SIV/IMV/COV visits, drive enrollment and data quality, resolve monitoring findings, maintain inspection-ready TMF/eTMF, and partner with cross-functional teams while mentoring CRAs.

Clinical Research Associate I at Cedars‑Sinai’s Smidt Heart Institute supports groundbreaking cardiovascular studies. Working closely with coordinators, program administrators, and nurses, the associate evaluates and abstracts data from source documents, completes Case Report Forms (CRFs), and enters information into sponsor‑provided Electronic Data Systems (EDCs).

Cedars‑Sinai seeks a Clinical Research Associate I for its Butte Lab in Los Angeles. The role supports translational bio‑photonics trials, coordinating patient visits, data entry, IRB submissions, and sample handling.

IQVIA’s Clinical Research Associate team drives site monitoring and management to ensure compliance with GCP and ICH guidelines. The role conducts site visits, manages recruitment plans, and maintains Trial Master Files while coordinating with study teams.