- Charles River Laboratories (South San Francisco, CA)
- …+ Maintain documentation for QA including but not limited to temperature strips, room environmental reports and logs, dish washer and/or autoclaving logs. + Handle ... safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space. **About… more
- Charles River Laboratories (San Diego, CA)
- …house animals according to SOP and Animal Receiving Form + Understand proper room entry order and adhere to biosafety requirements. + Maintain accurate records ... safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space. **About… more
- Abbott (Alameda, CA)
- …forms (CRFs), conducting User Acceptance Testing (UAT), Contract Research Organization ( CRO ) selection and management, selection and training of investigator sites, ... in conducting medical device and/or _in-vitro_ diagnostics studies preferred. Pharmaceutical background may also be considered. **Skills** + Demonstrated excellence… more
- Bristol Myers Squibb (San Diego, CA)
- …based on existing policy and procedures. + The Senior MSL will support CRO sponsored studies as agreed with leadership of clinical development and medical affairs. ... leaders. + Skilled in clinical research and understand the process of pharmaceutical product development and approval + Demonstrated ability to organize, prioritize,… more
- Grifols Shared Services North America, Inc (Los Angeles, CA)
- …and treatment questions in collaboration with the contract research organization ( CRO ) medical monitor, or directly with study investigators + Work closely ... feasibility and strategy or related experience. Additional experience may include other pharmaceutical or academic research in the field. + Hands-on experience with… more
- Actalent (San Francisco, CA)
- …study protocols and amendments, and lead document review and coordination. + Oversee CRO and vendor selection, scope of work creation, and ensure compliance with ... + 7+ years of experience as a GLOBAL Clinical Trial Manager with a pharmaceutical or biotech company. + 5+ years of global experience within oncology (SOLID TUMORS!)… more
- Kelly Services (Irvine, CA)
- …discipline + At least 2 years of experience in the pharmaceutical /biotech/medical device/ CRO industry required; experience with clinical study management ... and clinical research contract negotiation highly preferred + Medical device experience is preferred; cardiovascular experience is a plus + Effective time management, organizational and prioritization skills + Strong project management skills with meticulous… more
- Bristol Myers Squibb (San Diego, CA)
- …and alert appropriate BMS personnel to any identified Adverse Events + Actively support CRO sponsored studies as agreed with home office medical and GDO and as ... **Experience Desired** + A minimum of 2 years working in a clinical and/or pharmaceutical environment + Prior MSL or clinical practice experience + Ability to work… more
- Terumo Neuro (Aliso Viejo, CA)
- …2. Minimum seven (7) years of clinical data- management experience in the pharmaceutical , device or CRO setting. 3. Previous supervisory experience. 4. Proven ... ability to prioritize and manage multiple tasks with conflicting deadlines in support of corporate goals and objectives. 5. Experience reviewing study planning documents such as Edit Check Specs, UAT scripts, Data Management Plans, Data Transfer Plans.… more
- Charles River Laboratories (San Carlos, CA)
- …house animals according to SOP and Animal Receiving Form + Understand proper room entry order and adhere to biosafety requirements. + Maintain accurate records ... safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space. **About… more