Clinical Research Coordinator Jobs in Sacramento, CA

Job Summary: Collects data for clinical trials research, following general directions. Supports the preparation of study documentation for submission to regulatory bodies (e.g., IRB) for pre-implementation review and approval. May support clinical trials activities and research lab operations. Completes timely and accurate documentation of all research activities (e.g., consent forms, reports), with limited guidance. Assists with the development and/or implementation of standard quality control…

Job Summary: Collects data for clinical trials research, following general directions. Supports the preparation of study documentation for submission to regulatory bodies (e.g., IRB) for pre-implementation review and approval. May support clinical trials activities and research lab operations. Completes timely and accurate documentation of all research activities (e.g., consent forms, reports), with limited guidance. Assists with the development and/or implementation of standard quality control…

Position Overview: The salary range for this position is $200,000-$440,000. This position includes membership in the https://aadocs.ucdavis.edu/policies/apm/apm-670.pdf The Department of Neurology at the University of California, Davis, is recruiting a clinically focused Movement Disorders Neurologist to join our growing academic practice. Appointments are available in the Clinical Neurology or Health Sciences Clinical Professor series at the Assistant, Associate or Professor rank. RESPONSIBILI…

Imagine how your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy group…

Full-time Description The Research Department Supervisor oversees the coordination and management of clinical research studies, ensuring compliance with study protocols, institutional policies, FDA regulations (CFR), and ICH Good Clinical Practice (GCP). This role leads all phases of clinical trials, from design through closeout, and supervises research staff to ensure efficient, compliant operations. The supervisor works closely with Principal Investigators (PIs), central research teams, spons…

Company : Highmark Inc. Job Description : JOB SUMMARY This job is responsible for developing plans and managing activities in support of Risk Adjustment and Quality/HEDIS. Directs the daily activities of direct reports supporting Risk Adjustment Coding and Quality/HEDIS. Assesses viability of current direction/projects/operations and recommends strategies and tactics to satisfy current and future business needs. Actively seeks and identifies opportunities for improvement. Implements strategic a…

PXL FSP - Join an organization shaping smarter, faster clinical development PXL FSP is seeking a detail-oriented and proactive Feasibility Study Manager to support the delivery of high-quality global feasibility assessments. This role is ideal for someone who thrives in a fast-paced, data-driven environment and enjoys collaborating cross-functionally to ensure clinical programs launch with the strongest foundation possible. Key Responsibilities Survey Design & Configuration Transform draft fea…