- Abbott (Santa Clara, CA)
- …imaging catheters and software, vessel closure devices and peripheral stents. This ** Regulatory Affairs Manager ** position is an onsite opportunity working out ... based upon regulatory changes + Support pre and post approval clinical strategy and submission activities + Anticipate regulatory obstacles and emerging… more
- Abbott (Pleasanton, CA)
- … regulatory guidelines, policies and regulations + Ethical guidelines of the regulatory profession, clinical research and regulatory process ... executives, and scientists **The Opportunity** We are seeking a ** Regulatory Affairs Manager ** to join Abbott's Heart Failure Division on-site in Pleasanton,… more
- Oura (San Diego, CA)
- …human research studies that fuel our R&D. We're hiring an experienced Senior Research Project Manager to lead and scale this core function in the San ... collection and key meetings.. What you will do: + Lead cross-functional research study execution-including budgets, contracts, IRB and regulatory submissions,… more
- University of Southern California (San Diego, CA)
- … trials. The ATRI is seeking a motivated, dependable, and experienced Senior Project Manager to support ATRI clinical research efforts. The Senior Project ... monitoring. Minimum Skills: Industry experience in a pharmaceutical, biotechnology, clinical research organization and/or nursing setting. Demonstrated… more
- University of Southern California (San Diego, CA)
- …to: + Oversees Clinical Monitors for sponsor and investigator initiated clinical research + Responsible for managing study site assignments, daily ... as substitute for minimum education Minimum Experience: 5 years Minimum Skills: Extensive clinical research experience, and experience monitoring clinical … more
- BeOne Medicines (San Mateo, CA)
- …Applications **Other Qualifications:** + 6 or more years of progressive experience in clinical research within biotech, pharma or CRO industry + Proven ... progress in the region to senior management and Global Clinical Study Manager as required + Represents...experience in clinical research including relevant experience as team… more
- Sumitomo Pharma (Sacramento, CA)
- …of clinical study-related documents such as protocols, protocol amendments, clinical study reports (CSRs), regulatory submissions and other publications as ... early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients...and problem solving + Working knowledge of current global regulatory requirements and guidelines for clinical trials.… more
- Terumo Neuro (Aliso Viejo, CA)
- …writing, case report forms, and associated procedures. + Participate on corporate global clinical research teams ensuring that colleagues are updated on all ... **12521BR** **Title:** Sr. Manager , Clinical Data Management **Job Description:**...with development, validation, execution, maintenance, documentation, and archival of clinical data targeted for regulatory submission. 6.… more
- Sumitomo Pharma (Sacramento, CA)
- …. We are currently seeking a motivated and experienced individual for the position of Clinical Data Manager . The ** Clinical Data Manager (CDM)** is ... database modifications). + Collaborate with internal teams, which may include Clinical Operations, Research , Medical Monitoring, Medical Writing, Clinical… more
- Edwards Lifesciences (Irvine, CA)
- …need (Required):** + Bachelor's degree and 5 years of previous related experience in clinical research including clinical data management and/or clinical ... be part of our inspiring journey. As the **Senior Clinical Data Manager ** , you will ensure...field and 7 years of previous related experience in clinical research including clinical data… more