- AbbVie (San Francisco, CA)
- …one aspect of Drug Development (eg, pre-clinical research, clinical development, Regulatory Affairs , Chemistry Manufacturing and Controls (CMC)). + Experience ... part of the Corporate Strategy Office and actively supports global Business Development (BD) goals by sourcing and assessing...the science behind each of these opportunities. The Associate Director , Search & Evaluation will be a key member… more
- Edwards Lifesciences (Irvine, CA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
- J&J Family of Companies (Santa Clara, CA)
- …teams including but not limited to R&D, Supply Chain/Manufacturing, Clinical and Medical Affairs , Regulatory Affairs , Service, Marketing, in furthering new ... our Monarch platform. This role will directly report to Global VP of Q&C Robotics and Digital Surgery and...but not limited to R&D, Operations, Commercial, Supply Chain, Regulatory Affairs , Medtech/Enterprise, to assure quality and… more
- Ascendis Pharma (Palo Alto, CA)
- …validated Drug Safety Databases (Argus preferred) + Experience with MedDRA coding and global safety reporting regulatory requirements. + Expert knowledge of FDA ... safety regulations, ICH Guidelines, and other applicable regulatory guidance documents; working knowledge of global safety regulations. + Ability to travel up to… more
- Danaher Corporation (Sunnyvale, CA)
- …member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Cepheid is ... possible. The Senior Clinical Research Scientist reporting to the Director , Clinical Research, develops and independently writes clinical documentation including… more
- AbbVie (Irvine, CA)
- …cross-functional colleagues who support clinical trial execution and the Development and Global Medical Affairs Therapeutic Area MDs/SDs. + Key contributor to ... Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Clinical Operations Program Director is responsible to connect science and operations to bring… more
- Ascendis Pharma (Palo Alto, CA)
- …knowledge of FDA, EMA PV regulations, ICH Guidelines, and other applicable regulatory guidance documents; working knowledge of global safety regulations. + ... Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe,...laws and regulations and as appropriate, local and foreign regulatory reporting requirements and for signal detection, evaluation and… more
- Ascendis Pharma (Palo Alto, CA)
- …validated Drug Safety Databases (Argus preferred) + Experience with MedDRA coding and global safety reporting regulatory requirements. + Working knowledge of FDA ... safety regulations, ICH Guidelines, and other applicable regulatory guidance documents; working knowledge of global safety regulations. + Potentially may require… more
- Abbott (Santa Clara, CA)
- …stake holders including clinical project management, clinical operations, biostatistics data management, regulatory affairs , medical affairs as well as ... Abbott is a global healthcare leader that helps people live more...closely within the clinical study team including the medical director , biostatistician, project management, data management, and other clinical… more
- Abbott (Sylmar, CA)
- …functions such as compliance, legal, contracts & pricing, procurement, legal operations, regulatory affairs , governmental affairs , audit, and/or finance. + ... Abbott is a global healthcare leader that helps people live more...performs the following with moderate supervision from the OEC Manager/ Director + Supports and communicates with the business to… more