- BeOne Medicines (Emeryville, CA)
- …and safety section for clinical data management plan for capture during clinical trials , supports the review and update of data management plan based ... of safety data required for capture in CRFs during clinical trials , reviews and provides product program...(PAC) proposals, facilitates the design of PAC proposed safety study , executes PAC studies + Leads and… more
- Sumitomo Pharma (Sacramento, CA)
- …and Product Complaints (PCs) + Contributes to medical safety of clinical trials , including monitoring of clinical trial safety and laboratory data. ... marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs),… more
- ThermoFisher Scientific (San Diego, CA)
- …beyond through research , development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of ... novel frameworks for clinical research through our PPD ... portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver… more
- Astellas Pharma (South San Francisco, CA)
- …the research environment at the US site, promoting more efficient non- clinical research in collaboration with local members. **Responsibilities** 1. Plan and ... independently conduct appropriate in vitro non- clinical pharmacological studies , necessary to advance incubation-stage...experience: track record of advancing projects from discovery into clinical trial as non- clinical pharmacological… more
- IQVIA (Carlsbad, CA)
- …Associate! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor ... needs are met. Training & Communication: Provide protocol and study training to sites, maintaining regular communication to manage...from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …Real World Data Analytics organization to provide statistical expertise for analysis of clinical trials data beyond the study endpoints, including secondary, ... concept, protocol and SAP development for Real World Studies and ensure appropriateness of study design,...methods to support evidence generation. + Solid understanding of clinical research data standards, eg CDISC, ADaMs/STDMs.… more
- IQVIA (San Francisco, CA)
- …bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key ... role in ensuring the successful execution of clinical trials . In this position, you will...will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct… more
- Stanford University (Stanford, CA)
- …leads an Early Drug Development (EDD) Program focused on Phase I clinical trials in oncology. These are typically studies where first in-human novel cancer ... specialist in medical oncology, with a focus on early-phase clinical trials . Additionally, she or he should...are developed for our patients, incorporating biomarkers in their clinical design. Increasingly, these Phase I studies … more
- Bristol Myers Squibb (Los Angeles, CA)
- …BMS-sponsored clinical trials by identifying appropriate clinical trial sites, interacting with investigators in ongoing studies , and educating the ... community for referrals + Provide recommendations and insights to clinical development team on study and site...perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of… more
- University of Southern California (San Diego, CA)
- …the development of new treatments for Alzheimer's Disease (AD) through innovative clinical trials . Quality Assurance Specialist is responsible for the day-to-day ... program through which staff involved in the conduct of clinical research , therapeutic and non-therapeutic protocols, will...that essential documents are received and maintained across assigned studies + Participate in Study Team meetings… more