- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …associated disciplines, including immunology, biostatistics, clinical pharmacology, formulation science, data management , and medical writing. + Experience with ... and clinical study and safety documents. + Involved in product life cycle management from the earliest stages of development, constantly seeking innovations to add… more
- Vera Therapeutics (Brisbane, CA)
- …with a cross functional team and key personnel including clinical research, biostats, data management and medical writing, the CPA works collaboratively to ... support the operational components of global clinical trial management and potentially vendor management during study start up, conduct and close out under… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- **Job Summary** Under the direction of the Director/Associate Director of Clinical Management , the Senior Clinical Study Manager is responsible for the oversight and ... management of Otsuka clinical studies, including coordination with other...forecast to the Director/Associate Director.** **Establish communication flow with CRO and investigative sites to maximize compliance with study… more
- J&J Family of Companies (Santa Clara, CA)
- …reviewing safety sections of clinical study documents. This may also include management of Clinical Events Committee(s) and Data Safety Monitoring Board(s). ... to safety vendor(s), escalating vendor management issues as appropriate + Management of Clinical Events Committees (CEC) and Data and Safety Monitoring… more
- San Jose State University (San Jose, CA)
- Master's of Medical Product Development Management - Special Sessions Lecturer Pool Apply now ... - Health Sciences Department Summary The Master of Medical Product Development Management (MPDM) degree focuses on preparing students for an advanced career in… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …the highest quality and meet global regulatory reporting timelines. Responsible for data review, compilation and analysis including management of the integrated ... safety database. **_Essential Job Duties:_** + Management of Adverse Events including activities such as processing...in pharmacovigilance, clinical research, or regulatory affairs in a CRO or a pharmaceutical company is usually required. +… more
- NTT America, Inc. (San Francisco, CA)
- …customers, leveraging NTT DATA resources such as Marketing, Consulting, and the CRO office. + Generate, contribute, track, and manage new sales and account plan ... **Req ID:** 278785 NTT DATA strives to hire exceptional, innovative, and passionate...deliver comprehensive solutions to customers. + Provide feedback to management on market trends, competitive threats, and opportunities for… more
- Bristol Myers Squibb (San Diego, CA)
- …Clinical Development Lead/Clinical Trial Physician for provision and analysis of data to support future planning) **Position Responsibilities** + Maintain a thorough ... primary contact for clinical questions + Activities related to data generation and validation, including CRF design, clinical ...required by Protocol Manager for development of trial budget, CRO scope of work, etc. + Review development of… more
- NTT America, Inc. (San Francisco, CA)
- **Req ID:** 303568 NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, ... to join our team in San Francisco, California (US-CA), United States (US). NTT DATA 's Launch business unit is looking for a Launch Industry Solution Expert for… more
- Organon & Co. (Sacramento, CA)
- … data science, clinical operations, regulatory affairs, chemistry, manufacturing and control (CMC), project management and other partner groups as part ... internal (biostatistics, clinical operations) and external (contract research organization [ CRO ], bioanalytical and/or modeling vendors) colleagues. The Clinical Pharmacology… more
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