- Houston Methodist (Houston, TX)
- … with ethical and legal business practices and accreditation/ regulatory /government regulations. **PEOPLE ESSENTIAL FUNCTIONS** + Performs management responsibilities ... At Houston Methodist, the Manager Clinical Trials position is responsible for managing complex...projects to include quality of services, timelines, financial viability, compliance with federal, state and/or other regulations, laws and… more
- Penn Medicine (Woodbury Heights, NJ)
- …for the office and generates front-end process reports as requested. Other / Regulatory : + Ensures compliance with all applicable federal, state, and local ... Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate (Fixed-term 12 months) **School of Medicine, Stanford, California, United States** **New** Research Post Date 2 days ago ... research, encompassing a wide spectrum of programs in basic, translational, clinical , health services and medical education. The Department of Anesthesiology,… more
- ICON Clinical Research (San Antonio, TX)
- … clinical research activities in accordance with study protocols, regulatory guidelines, and standard operating procedures (SOPs). + Conducting patient ... effectively with healthcare professionals and study investigators. + KNwledge of regulatory requirements governing clinical research, including the International… more
- AdventHealth (Orlando, FL)
- …assigned service line's clinical program performance as well as regulatory compliance and accreditation requirements. The manager facilitates the development ... the clinical program content expert through skilled knowledge of clinical evidence-based guidelines, national accreditation standards and regulatory (state… more
- Lilly (Indianapolis, IN)
- …trial sites, drawing on strong medical and scientific knowledge/principles, understanding of compliance and regulatory requirements as well as awareness across ... interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other… more
- Stanford University (Stanford, CA)
- Cancer Clinical Research Coordinator Associate - GI (Hybrid) **School of Medicine, Stanford, California, United States** Research Post Date Aug 29, 2025 Requisition ... # 106962 **Cancer Clinical Research Coordinator Associate - GI Oncology** The Stanford...Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. +… more
- Sanofi Group (Cambridge, MA)
- …with the global project team and internal partners such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, ... clinical study protocol + Oversee the execution of clinical studies in compliance with internal SOPs,...ICH guidelines and other regulations + Review documents supporting clinical development such as Investigator's brochure, regulatory … more
- Sanofi Group (Morristown, NJ)
- …with the global project team and internal partners such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, ... an abbreviated and full clinical study protocol. + Oversee the execution of clinical studies in compliance with internal SOPs, GCP, ICH guidelines and other… more
- Gilead Sciences, Inc. (Foster City, CA)
- … trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that ... and reviews routine regulatory documents to ensure that CROs are in compliance with protocols, regulatory requirements, SOPs, and monitoring plans. + May be… more