- Cordis (Irvine, CA)
- …Perform other duties as assigned. + Interface with Operations Management to review project goals and priorities + Formulate the sustaining activities for the ... work experience + 5+ years' experience in the medical device/ pharmaceutical field or in a related area. + Excellent...interact with all levels of management. + Ability to review and write/edit technical documents. + Strong Root Cause… more
- Kelly Services (Irvine, CA)
- …seeking a Technical Writer 1 for a long-term engagement with one of our Global Pharmaceutical clients. This position is onsite 2-3 days per week in Irvine, CA. This ... level suitable for the intended audience. + Analyzes and review the preparation and organization of complex research. +...to various projects and prepares reports of changes for review . + Organizes and coordinates assignments that involve complex,… more
- Datavant (Sacramento, CA)
- …in the healthcare sector + Application of RWD and RWE in the pharmaceutical and life sciences space + Understanding of drug development and/or clinical trials ... protected status. To learn more about our commitment, please review our EEO Commitment Statement here (https://www.datavant.com/eeo-commitment-statement) . Know Your… more
- Gilead Sciences, Inc. (Foster City, CA)
- …as modular content development, AI-enhanced content creation, and evolving content review processes-ensuring their adoption within Global Strategic Marketing. As new ... across markets. + The individual will also shape how the global content review process evolves to support these new ways of working, ensuring it remains… more
- BeOne Medicines (San Mateo, CA)
- …Functions of the Job:** + Facilitate generation of, author, update, and/or review key documents, including, but not limited to: + Protocol concepts, synopses, ... to clinical questions from sites, IRBs/IECs, Health Authorities, and CRO's + Review , query, and analyze clinical trial data. + Interpret, and present clinical… more
- EMCOR Group (Anaheim, CA)
- …manufacturing facilities, clean rooms, cGMP facilities and process systems for Pharmaceutical and microelectronics facilities is desired. Ability to produce a ... set the specific duties and responsibilities for each employee. Bid document review , pre-bid meetings, client interface, plumbing system sizing and layout from… more
- BeOne Medicines (San Mateo, CA)
- …Functions of the job:** + Facilitate generation of, author, update, and/or review key documents + Protocol concepts, synopses, protocols, and amendments + Informed ... respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CROs + Review , query, and analyze clinical trial data + Interpret, and present clinical… more
- US Tech Solutions (CA)
- …social media **content creation,** digital storytelling Client Company, the fourth largest pharmaceutical company in the world. We have a duty to provide training ... for collaboration with key stakeholders (AMI Programs team, Brand teams, Internal review team, etc) to **create and design educational materials** for the Medical… more
- University of Southern California (San Diego, CA)
- …resolving data quality problems across various sources. + Data Cleaning: Perform data review data cleaning and root cause analysis, query generation in the data ... as per the Edit Check Specifications. + Performs eTMF review and loading of study documentations in the eTMFs....1.5 years of experience in clinical trials at a pharmaceutical , biotechnology, or academic clinical research institute or on… more
- Florida Crystals Corporation (Crockett, CA)
- …limits. Develops future talent and leadership. Provides reports to VP/GM to review progress against goals. POSITION RESPONSIBILITIES + Ensures safety and regulatory ... of bottlenecks and the proposals to eliminate. + Helps develop, review , modify and implement operating systems in sanitation, safety, quality, preventative… more