- BeOne Medicines (San Mateo, CA)
- … questions from sites, IRBs/IECs, Health Authorities, and CROs. + Review, query, and analyze clinical trial data . + Interpret, and present clinical trial ... selection of investigator and vendors. + Train BeiGene colleagues, CRO staff, and study site staff on the therapeutic...data both internally and externally. + Represent a clinical study or development program on one or more… more
- Organon & Co. (Sacramento, CA)
- …with cross-functional colleagues in preclinical science, data science, clinical operations, regulatory affairs, chemistry, manufacturing and control (CMC), ... 1 to 2a study protocols, in collaboration with internal (biostatistics, clinical operations) and external (contract research organization [ CRO ], bioanalytical… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …to add value strategically. + Provides strategic oversight in our vendor and CRO relationships and provides clinical input into their governance committees. + ... + Working knowledge of associated disciplines, including immunology, biostatistics, clinical pharmacology, formulation science, data management, and medical… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …innovations to add value. + Provide strategic oversight in our vendor and CRO relationships and provide clinical input into their governance committees. + ... + Working knowledge of associated disciplines, including immunology, biostatistics, clinical pharmacology, formulation science, data management, and medical… more
- Bristol Myers Squibb (San Diego, CA)
- …Payment) + Provide scientific support at promotional meetings by presenting scientific and clinical data , by evaluating speakers and by giving support to ... personnel to any identified Adverse Events + Actively support CRO sponsored studies as agreed with home office medical...act as a team player + Translating scientific or clinical data into an understandable and valuable… more
- Bristol Myers Squibb (San Diego, CA)
- …competitive landscape and patient treatment trends + Ability to translate scientific or clinical data into an understandable and valuable form to help physicians ... will support CRO sponsored studies as agreed with leadership of clinical development and medical affairs. **Education and Experience** + A doctorate degree… more
- J&J Family of Companies (Santa Clara, CA)
- …of clinical study documents. This may also include management of Clinical Events Committee(s) and Data Safety Monitoring Board(s). **Essential Job ... escalating vendor management issues as appropriate + Management of Clinical Events Committees (CEC) and Data and...sites, as needed + Liaison for safety-related questions from Clinical Affairs, CRO , monitors, Field Clinical… more
- BeOne Medicines (San Mateo, CA)
- …a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance ... Word, Excel, PowerPoint and Outlook * Familiar with industry CTMS and data management systems **Other Qualifications:** * Understands clinical trial processes… more
- AbbVie (South San Francisco, CA)
- …Director, Statistical Programming leads the whole stat programming team within CDOR ( Clinical Data Operation and Reporting) in OED (Oncology Early Development) ... clinical development organization.The stat programming team performs statistical programming...and lead stat programming related process improvement collaborating with CRO partners, create a collaborative team work environment for… more
- Terumo Neuro (Aliso Viejo, CA)
- …producing some of the most reliable and technologically advanced products supported by proven clinical data . Take a closer look at what **Micro** Vention (R) ... Some typical job duties include: + Collaborating with the clinical & regulatory teams to write clinical ... submissions (preferably as a medical writer for pharmaceutical, CRO , or medical device clients). 4. Excellent writing and… more