- Gilead Sciences, Inc. (Foster City, CA)
- …broad cross functional leadership. Manage cross-functional collaboration processes to ensure development of insightful market research plans that systematically ... priorities of the commercial business. + Direct activities to support the professional development of the HIV Prevention Market Research team and support… more
- J&J Family of Companies (Irvine, CA)
- …Discovery & Pre-Clinical/Clinical Development **Job Sub** **Function:** Clinical Development & Research - Non-MD **Job Category:** Scientific/Technology ... with internal teams: medical affairs, data management, biostatistics, data programmers, and regulatory affairs + Ensure clinical research studies follow … more
- Rhythm Pharmaceuticals (Boston, MA)
- …of non-clinical studies supporting IND, early clinical development , and regulatory submissions. + Represent non-clinical research in regulatory ... role requires extensive cross-functional engagement with senior leaders in clinical development , regulatory affairs, data sciences, and commercial functions to… more
- Lilly (Stamford, CT)
- …to make life better for people around the world. **Position Overview:** The ** Development Clinical Research Scientist** (CRS) in the **Breast Cancer Franchise** ... regulatory documentation. **Primary Responsibilities** + Contribute to the development and execution of clinical strategies for breast cancer programs. Maintain… more
- Stanford University (Stanford, CA)
- …maximizing the budget, ensuring appropriate care of major equipment, and addressing regulatory and administrative requirements. The Research Scientist will write ... Basic Life Research Scientist (1 Year Fixed Term) **School of...The Ross Lab is led by Jason Ross, MD, PhD , and is situated within the Stanford University School… more
- Stanford University (Stanford, CA)
- …projects. Supervise multiple clinical research staff. Manage clinical research operations, including quality management, personnel management, regulatory ... + Proficiency with Microsoft Office and database applications. + Experience with research protocols and regulatory or governing bodies, which include HIPAA… more
- University of Colorado (Aurora, CO)
- … Research Participant Progress Reports (RPPR) + Experience managing regulatory requirements related to human subjects research , including experience ... ** Research Services Manager / Research Manager**...of Minnesota and University of Georgia), including planning, protocol development , budget oversight, and timeline management. + Develop and… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …for conferences, corporate locations, and stakeholder meetings. Educational Qualifications: + PhD or Masters in Health Economics, Outcomes Research , Health ... Services Research , Public Health or related discipline + Three ( PhD ) to five (Masters) years of relevant experience **Competencies** **Accountability for Results… more
- Merck (Boston, MA)
- …development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May Be ... study reports, or publication + Participation in internal and joint internal/external research project teams relevant to the development of new compounds,… more
- Merck (Boston, MA)
- …post-licensure). The Director will manage the entire cycle of clinical development , including study design, initiation, monitoring, analysis, regulatory ... study reports, or publication; and + Participation in internal and joint internal/external research project teams relevant to the development of new compounds,… more