Clinical Research Associate Jobs in California, United States

Clinical Research Data Associate II manages data for oncology studies, designs data collection forms, abstracts clinical data, processes and cleans data, produces reports, supports audits, trains staff, and performs basic statistical analysis with biostatisticians.

The Angeles Clinic & Research Institute, part of Cedars-Sinai Medical Center, seeks a Clinical Research Data Associate II to manage data for assigned research studies in Los Angeles. This hybrid role involves designing data collection forms, performing clinical data abstraction, processing data, and producing project reports while ensuring regulatory compliance.

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.

ADC Diabetes Care at Abbott focuses on innovative diabetes management solutions. The Clinical Research Associate I assists in planning, executing, and managing clinical studies, including site qualification visits, regulatory document collection, device shipment coordination, and trial master file maintenance.

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

Clinical Research Team at Cedars-Sinai Medical Center supports non‑complex clinical studies by collecting data, managing participant scheduling, and ensuring regulatory compliance. The Clinical Research Associate I assists coordinators with data entry into EDC systems, IRB submissions, budget tracking, and sample handling.

VahatiCor’s Clinical Research Associate drives monitoring and site engagement for cardiovascular device trials, ensuring compliance with FDA, ICH/GCP, and SOPs. The role conducts routine and remote visits, verifies source data, maintains TMF, and collaborates with CTMs, data management, and vendors to support study execution.

IQVIA seeks a Clinical Research Associate to ensure sites conduct studies and report data per protocol, regulations, and sponsor requirements. The role involves performing site monitoring visits, managing recruitment plans, and maintaining regulatory documentation like the Trial Master File.

Senior Associate, Clinical Research at JENAVALVE TECHNOLOGY INC. Supports pre‑market clinical studies, ensuring GCP compliance, data quality, and regulatory documentation. Manages site coordination, EDC training, Trial Master Files, audits, and vendor relationships.

Clinical Research Associate on Merck's Oncology team, responsible for ensuring compliance and performance of clinical trial protocols across assigned sites. The role conducts site monitoring, manages regulatory documentation, and collaborates with cross‑functional teams to support study start‑up, execution, and close‑out.

Clinical Research Associate on IQVIA’s Sponsor Dedicated team, ensuring sites conduct studies per GCP and ICH guidelines. The role monitors visits, drives recruitment, trains sites, evaluates quality, tracks regulatory submissions, maintains TMF, and manages financials.

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.

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.

Clinical Operations team at Epicrispr Biotechnologies drives the execution of biotech clinical trials. The Senior CRA ensures GCP compliance, manages site activities, oversees sample logistics, and partners with CROs to maintain data quality and protocol adherence.

Diabetes Care division at Abbott focuses on innovative diabetes management solutions. The Clinical Research Associate II assists in execution and management of clinical studies, conducts site selection, qualification visits, and ensures trial documentation readiness.

Merck seeks a Clinical Research Associate to manage assigned protocols and sites within Immunology, ensuring compliance with ICH/GCP and country regulations. The role involves acting as the primary site contact, performing remote and on-site monitoring, and developing new clinical research territories across designated US locations.

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.

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 team at Merck conducts oncology trials across the United States. The Clinical Research Associate ensures protocol compliance, manages site relationships, and performs remote and on‑site monitoring while coordinating with cross‑functional partners.

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, administers protocol training, and maintains Trial Master File documentation across multiple U.S. locations.