- BeOne Medicines (Emeryville, CA)
- …+ Provide guidance to the CST and ensure timely, quality, and efficient study planning and execution of associated clinical programs/ studies + Conduct regular ... lead and manage the Global Clinical Program Lead (GCPL)/ Global Clinical Study Manager (gCSM) group in designated Franchise(s)- therapeutic area (s) or asset(s),… more
- Parexel (Glendale, CA)
- …do after training is completed** (including but not limited): + You will understand study protocols and be able to complete required medical procedures. + Recruit ... study participants by calling the database, attending company sponsored...schools, senior centers, supermarkets, and other establishments. + Enter study participants in the study participant tracking… more
- Cedars-Sinai (Beverly Hills, CA)
- …is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, ... interfaces with participants and family members. Coordinates the clinical logistics of the study , and works in tandem with the Research and/or Clinical Nurse who… more
- BeOne Medicines (Emeryville, CA)
- …and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP ... and applicable SOPs. The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical... Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other… more
- Parexel (Sacramento, CA)
- …Partner is a crucial liaison for investigative sites throughout a study 's lifecycle, responsible for site start-up, activation, relationship management, recruitment, ... + Maintains a knowledge of assigned protocols + Conducts study start-up activities at the site level including but...relationships with Site Organizations and Strategic Partners + Provides study support on escalated site issues related to … more
- Parexel (Sacramento, CA)
- …clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices ... Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the...of sites in a clinical trial. **Monitoring Responsibilities and Study Conduct:** + Ensure proper conduct of clinical trials… more
- Stanford University (Stanford, CA)
- …in clinical trials. Assess physical health and administer treatments throughout the study aligned with scope of practice delegated responsibilities. Oversee study ... participant safety. . **Duties include:** + Ensure the safety of study participants, and maintain communication with their families/caregivers and clinicians. +… more
- Stanford University (Stanford, CA)
- …Wu Tsai Human Performance Alliance's Human Performance Lab and an ongoing, large-scale study to screen athletes for risk of anterior cruciate ligament injury. This ... outdoors. **CORE DUTIES** **:** + Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research… more
- BeOne Medicines (San Mateo, CA)
- …provide strategic statistical leadership for pharmacokinetic (PK) and pharmacodynamic (PD) studies across all phases of clinical development. This role partners ... Clinical Biomarker, Regulatory Affairs, and Clinical Development to ensure robust study design, insightful data analysis, and timely support for global regulatory… more
- Cedars-Sinai (Los Angeles, CA)
- …to assist in tasks supporting the coordination/implementation of noncomplex research studies . Supports objectives of research studies through noncomplex tasks ... to assist in tasks supporting the coordination/implementation of noncomplex research studies . + Collects, evaluates and/or abstracts clinical research data. May… more