- Baylor Scott & White Health (Dallas, TX)
- …Rehabilitation assists various Principal Investigators (PI), through delegated authority, in conducting clinical trials during all phases of trials including ... different project workflows based on the needs of the clinical trial protocol. Examples of workflows include,...study budgets and provides feedback on budgets for new clinical trials . Performs research subject informed consent… more
- Gilead Sciences, Inc. (Foster City, CA)
- …associated capabilities to support the CDS objectives + Manage quality review of clinical trial documents, workflows, and outputs within the CDS organization to ... ensure clinical trials are conducted in compliance with Gilead procedures, GCP and applicable global regulations + Analyze trends to identify process gaps,… more
- Actalent (Merced, CA)
- …with Principal Investigators and sponsors + Drive PI engagement and site-level trial success Qualifications + 3+ years of clinical research experience ... Clinical Research Coordinator - Oncology Focus (Merced, CA)...Responsibilities + Lead coordination of lung and breast cancer trials (6-7 studies planned) + Manage IRB submissions, informed… more
- Genentech (South San Francisco, CA)
- …7+ years experience in pharmaceutical/biotech clinical data management / Biometrics ( clinical trial data and/or Real World Data) + Demonstrated collaboration ... teams, overseeing trial data activities, and collecting clinical trial and/or Real World Data, with...**Preferred:** + Medical affairs experience (Phase IIIB - IV trials experience) + Proficiency in programming languages such as… more
- SUNY Upstate Medical University (Syracuse, NY)
- …entry and query resolution. The CRA I will be the point person on assigned clinical trials and flexible availability is expected. This role is also the key ... Job Summary: The Clinical Research Associate I (CRA I) will join...a team of experienced associates and manage various research trials , including first in human through phase 3 … more
- SUNY Upstate Medical University (Syracuse, NY)
- …and regulatory agencies. Enroll, register and screen patients for clinical research trials ; collect and submit clinical trial patient data. Perform ... Job Summary: Coordinate various research trials for the Institute for Global Health, including...and shipment of lab samples; billing support; maintenance of clinical research study supplies and drug accountability. Minimum Qualifications:… more
- University of Pennsylvania (Philadelphia, PA)
- …Summary This position will be a resource for best practices of managing major clinical trials . The coordinator will provide guidance to both study trials ... to other members of the team and will oversee the implementation of new clinical trials . Will review all new trials to help identify the challenges and… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …**The Role** + Monitors, organizes and performs all functions associated with packaging of clinical trial supplies and assures compliance to GMPs, SOPs, FDA, DEA ... Clinical , contract or production experience required + Clinical Trial Manufacturing and Packaging experience preferred...sizes to advance new medicines from early development to clinical trials and to the market. Catalent… more
- Cedars-Sinai (Los Angeles, CA)
- …as needed. + Work with bioinformatics in the development and maintenance of clinical trials management systems including validation of systems, as needed. + ... with cancer. **Join our team and contribute to groundbreaking research!** The Clinical Research Data Associate III manages the data for assigned research studies.… more
- Cedars-Sinai (Los Angeles, CA)
- …Responsibilities: + Collaborates with bioinformatics in the development and maintenance of clinical trials management systems including validation of systems. + ... outcomes. **Are you ready to be a part of breakthrough research?** The Clinical Research Data Specialist II independently manages data for assigned research studies,… more