- Philips (San Diego, CA)
- …awareness. + Ensures compliance with medical affairs activities, including Investigator Initiated Research and off-label requests, while adhering to regulatory ... Quality, Regulatory, and Clinical Affairs, to drive product advancement, ensure safety and performance, and support global publication plans through manuscript and… more
- Cedars-Sinai (CA)
- …etc.). Organizes clinical/research trials in conjunction with the Principal Investigator and sponsor and/or funding source. Monitors and ensures compliance ... with safety standards and procedures Analyzes data and prepares scientific findings for publication as author or co-author. May make independent presentations May… more
- Pfizer (South San Francisco, CA)
- …development and maintenance of clinical documents ( eg protocols and amendments, investigator brochures, clinical study reports) + Lead development of clinical study ... + Develop manuscripts, abstracts and presentations for scientific meetings + Evaluate safety , pharmacology, and efficacy data from ongoing and completed studies to… more
- Clear Labs (San Carlos, CA)
- …of assays, reagents and automated methods for our clinical and food safety platforms. You will be part of multidisciplinary teams solving complex problems, ... presentations, posters, and manuscripts under the direction of the Principal Investigator + Contribute proactively in data analysis and troubleshooting experimental… more
- Genentech (South San Francisco, CA)
- …mindset. They serve as the guardian for high standards of compliance, ethics and safety . **Key Responsibilities** **Who you are** + Co-own with the team, the medical ... execution of high quality Phase IIIb/IV clinical trials and investigator -initiated research including study design, protocol writing, approval, implementation and… more
- Bristol Myers Squibb (Brisbane, CA)
- …of clinical study protocols and related documents (eg, Informed Consent Forms, Investigator Brochures). + Support the design and implementation of clinical trials in ... for study design and endpoints. + Review and interpret clinical data, including safety and efficacy data, and identify trends or issues. + Draft, review, and… more
- Ascendis Pharma (Palo Alto, CA)
- …Ensure successful completion of documents (including clinical trial protocols, investigator brochures, monitoring plans, site training materials, clinical study ... across multiple endocrine projects + Ensure study integrity, and track accumulating safety and efficacy data + Anticipate obstacles within a clinical trial, and… more
- General Atomics (Poway, CA)
- …and mechanical design. **DUTIES AND RESPONSIBILITIES:** + Perform as the Principal Investigator (PI) for phased antenna array systems. + Lead or participate in ... with technical experience demonstrating the application of those concepts while ensuring safety and regulatory compliance. + Must have a strong understanding of… more
- Abbott (Alameda, CA)
- …products under development. + Participates in adverse event reporting and safety responsibilities monitoring. + Coordinates and provides reporting information for ... adherence to protocols and determines study completion. + Coordinates and oversees investigator initiations and group studies. + May act as consultant/liaison with… more
- Pfizer (South San Francisco, CA)
- …the development and management of clinical protocols and amendments, investigator brochures, clinical study reports, statistical analysis plan, and regulatory ... and Operations, Pharm Sci and Product Teams. + Oversee the evaluation of safety , pharmacology, and efficacy data from ongoing and completed studies for early… more