- Sumitomo Pharma (Sacramento, CA)
- …a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The associate ... on strong medical and scientific principles, knowledge of compliance and regulatory requirements, markets, business operations, and emerging issues. + Oversee… more
- Stanford University (Stanford, CA)
- …case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are ... Neuromuscular Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States**...neuromuscular disorders. * Are exceptionally organized and can balance multiple projects at one time. * Have excellent time… more
- Stanford University (Stanford, CA)
- …for the overall management and implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States**...forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Oct 24, 2025 Requisition # 107631 Stanford ... Department of Neurosurgery is seeking a Clinical Research Coordinator Associate (CRCA) to perform duties related to the coordination...enroll and follow patients on trial and assist with regulatory and financial requirements of the trials. We are… more
- Horizon Services, Inc. (Hayward, CA)
- JOB TITLE: Associate Director of Outpatient & Prevention Program Operations LOCATION: Administration - Hayward CA Employment Type: Full-Time (Salary) POSITION START ... community where our collective experiences enrich each other's growth. The Associate Director of Outpatient & Prevention Programs (ADOPPO) position is instrumental… more
- Parexel (Sacramento, CA)
- …for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at ... in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and… more
- Parexel (Sacramento, CA)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local ... in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and… more
- Parexel (Sacramento, CA)
- …workflows and projects and participate in safety processing for studies including medical review of serious adverse events. * Support regulatory safety reporting ... we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and Inflammation… more
- Gilead Sciences, Inc. (Foster City, CA)
- …With increasing independence, you will lead biostatistical analysis and reporting, document review and data inclusion for NDA submissions of assigned studies by ... input into clinical development documentation, scientific publications and presentations, and regulatory filings. Dependent upon the area of assignment, you may lead… more
- Stanford University (Stanford, CA)
- Director, Research Security ( Associate Director or Director) **Dean of Research, Stanford, California, United States** **New** Administration Post Date 3 days ago ... (the university's central resource for research-related policies) RPI provides policy and regulatory support in the following major areas: Conflict of Commitment and… more