- BeOne Medicines (San Mateo, CA)
- …and up to 2 studies in late development) + Seamless transition of drug candidates from research to early clinical development + Effective integration ... play a key role the establishment and growth of Clinical Research functions to assure best-in-class global...amendments + Informed consent documents + Investigator Brochures + Clinical study reports + Abstracts, posters and… more
- BeOne Medicines (San Carlos, CA)
- …+ Collaborate with and manage external vendors and collaborators involved in clinical studies or translational research , including vendor evaluation ... Biomarker Scientist to lead biomarker strategy and execution in clinical studies . The role involves designing and...+ Serve as the primary biomarker scientist for the clinical study team, ensuring biomarker strategies are… more
- BeOne Medicines (Emeryville, CA)
- …potential to apply their existing skills to oncology + Expert understanding of global clinical study design and drug development process from discovery to ... play a key role the establishment and growth of Clinical Research functions to assure best-in-class global...amendments + Informed consent documents + Investigator Brochures + Clinical study reports + Abstracts, posters and… more
- BeOne Medicines (San Mateo, CA)
- …potential to apply their existing skills to oncology. + Expert understanding of global clinical study design and drug development process from discovery to ... play a key role the establishment and growth of Clinical Research functions to assure best-in-class global...amendments o Informed consent documents; + Investigator Brochures o Clinical study reports; + Abstracts, posters and… more
- AbbVie (Irvine, CA)
- …key external meetings. *Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable ... study staff. *May have responsibility for leading clinical study teams, monitoring overall study...may include supervision of matrix team members; serving as Clinical Research representative to lend clinical… more
- Kelly Services (Thousand Oaks, CA)
- Job Title: Research Associate - In Vivo Pharmacology Job Summary: Our client is a pioneering biotech company focused on developing therapeutic solutions for ... neurological and cardiovascular diseases. As part of their expanding research team, they are seeking a Research ...with strong in vivo pharmacology expertise to support early-stage drug development. This contract role offers the opportunity to… more
- University of Southern California (San Diego, CA)
- …Skills: Extensive clinical research experience, and experience monitoring clinical research studies . Experience with medical terminology, and with ... Monitors for sponsor and investigator initiated clinical research + Responsible for managing study site...Preferred Experience: 10 years 6 years of experience monitoring clinical research studies . Preferred Skills:… more
- Bristol Myers Squibb (San Diego, CA)
- …order to gain their inputs on emerging science in drug and biomarker research , disease knowledge, and design of clinical development studies and programs ... organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical...studies + Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working… more
- University of Southern California (Los Angeles, CA)
- …California This position requires a person with a strong medical background and an interest in clinical research . The role of the Research Coordinator I is a ... questions regarding study and toxicities. c. Calculates correct dose of drug to be administered after determining the Body Surface Area (BSA). Subsequent dose… more
- Bristol Myers Squibb (San Diego, CA)
- …and strategic advice, and meet milestones and budgets + Translate findings from research and nonclinical studies into clinical development opportunities + ... partner with investigators and CROs to design and implement clinical studies + Contribute to writing of... + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other… more