- Robert Half Finance & Accounting (Roseville, CA)
- …+ Assist with financial statement audits, property and sales tax filings, and regulatory submissions . + Guide the implementation and improvement of accounting ... systems, internal controls, and financial policies as the company grows and enters new states. + Partner with cross-functional leaders on budgeting, forecasting, and ad hoc financial analyses to support strategic decision-making. + Mentor and supervise a… more
- Abbott (Alameda, CA)
- …enhancing data and analytics capabilities, supporting clinical trials, evidence generation, and regulatory submissions . + Ensure IT investments are aligned with ... business priorities, delivering measurable outcomes that advance innovation and operational resilience. + Strengthen foundational capabilities through robust data governance, cybersecurity, and lifecycle management to support secure and compliant operations.… more
- Bristol Myers Squibb (San Diego, CA)
- …data package development for clinical studies to support CSRs and future regulatory submissions + Create SAS macros/applications to streamline processes and ... enhance efficiency **Education and Experience** + A bachelor's degree required in statistics, mathematics or equivalent with at least 10 years' experience in pharmaceutical industry; or a master's degree in statistics or computer science with at least 7 years'… more
- WuXi AppTec (San Diego, CA)
- …planning; Plan, execute, and document cGMP and non-GMP/GLP laboratory work supporting regulatory submissions ; Assist with Scale up (multi-kg scale) tech ... transfers from Kilo Lab and Pilot Plant scales following cGMP compliant execution of API manufacturing processes; Research and recommend new methods and alternative synthetic sequence techniques to optimize existing processes (Process R&D); Perform… more
- Oura (San Francisco, CA)
- …Contribute to cross-functional team reviews, design iterations, and documentation needed for future regulatory submissions or quality assurance. + Act as a human ... factors expert and lay the foundation for this rich competency within Ōura's interdisciplinary design team. This is a hybrid-remote role, with the expectation to work from our San Francisco offices at least half-time. Requirements We would love to have you on… more
- Cedars-Sinai (Los Angeles, CA)
- …or patient contact for long-term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including submission ... of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. + Responsible for sample preparation and shipping and maintenance of study supplies and kits. + Maintains research practices using Good Clinical… more
- United Therapeutics (Sacramento, CA)
- …Knowledge of data entry processing, from start to finish (QC, medical review, regulatory submissions ) + Prior clinical or post marketing experience **Job ... Location & Travel** United Therapeutics has the flexibility to hire this role remotely with a 20% travel expectation, OR based in our Durham, NC office with a hybrid schedule of three to four days onsite each week and with a 10% travel expectation. Travel may… more
- Oura (San Diego, CA)
- …Lead cross-functional research study execution-including budgets, contracts, IRB and regulatory submissions , logistics, trouble-shooting, and data quality ... monitoring, for both internal and external studies. + Manage and grow a team of research coordinators-scale our in-house research study capabilities in the San Diego location + Expand our network of research partners-identify, vet, and build relationships with… more
- Stryker (Irvine, CA)
- …Will Do:** + Develop quality documentation to support new product development and regulatory submissions . + Maintain and improve quality systems by identifying ... and correcting procedural deficiencies. + Lead risk management activities and present final risk/benefit justifications to leadership. + Drive product and process design activities in cross-functional teams. + Define and validate design verification and… more
- Cedars-Sinai (Los Angeles, CA)
- …for long term follow-up patients only. + Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB) including submission ... of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines + Assists with clinical trial budgets and patient research billing + Responsible for sample preparation and shipping and maintenance of study supplies… more