Schedule: Monday - Friday 9:00 AM - 5:00 PM SUMMARY As a part of Clinical Trials Scientific Affairs, the Senior Principal... Scientist will lead method selection, development, validation, and implementation. The Senior Principal Scientist...
; Participates in clinical nutrition Continuous Quality Improvement (CQI) activities and completes one outcome study per year... study and provide treatment of conditions that affect glands and hormones that regulate metabolism, growth and development...
and interpret clinical study protocols to gather design requirements. Stakeholder Collaboration: Engage with internal teams...Location: Remote USA About Us: At Signant Health, we are dedicated to transforming clinical trials through innovative...
for our individual patients and our communities. The Department of Emergency Medicine is seeking a Senior Research Scientist to lead.... ☰ Senior Research Scientist (3-Year Fixed-Term), Emergency Medicine (U.S. - Flexible Work Location) New 📁 Research 📅...
University of Colorado Anschutz Medical Campus Department: Pediatric Hematology/Oncology/BMT Job Title: Senior...: Senior Laboratory Science Professionals perform duties in an experimental lab, or wet lab, and handle a variety of chemicals...
, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience leading and managing... teams while authoring regulatory documents with aggressive timelines Experience in regulatory submissions (clinical study...
, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience leading and managing... teams while authoring regulatory documents with aggressive timelines Experience in regulatory submissions (clinical study...
, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience leading and managing... teams while authoring regulatory documents with aggressive timelines Experience in regulatory submissions (clinical study...
, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience leading and managing... teams while authoring regulatory documents with aggressive timelines Experience in regulatory submissions (clinical study...
, and ICH guidelines a plus Substantial clinical study protocol experience, as lead author, required Experience leading and managing... a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline Substantial clinical study protocol experience...
, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience leading and managing... teams while authoring regulatory documents with aggressive timelines Experience in regulatory submissions (clinical study...
, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience leading and managing... teams while authoring regulatory documents with aggressive timelines Experience in regulatory submissions (clinical study...
, and ICH guidelines a plus Substantial clinical study protocol experience, as lead author, required Experience leading and managing... a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline Substantial clinical study protocol experience...
, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience leading and managing... teams while authoring regulatory documents with aggressive timelines Experience in regulatory submissions (clinical study...
that meet study analysis needs and requirements. The Analysis Oversight Statistical Programming (AOSP) Lead is essential... to these partnerships. As a member of the Study Management Team (SMT), the AOSP Lead works closely with the study team...
, their use in various clinical study designs, and supply sourcing strategies preferred Experience with blinded/masked studies... Supply Chain Operations and the Lead for Marketed Products Planning & Forecasting. This position will be responsible...
, and ICH guidelines a plus Substantial clinical study protocol experience, as lead author, required Experience leading and managing... a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline Substantial clinical study protocol experience...
, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience leading and managing... teams while authoring regulatory documents with aggressive timelines Experience in regulatory submissions (clinical study...
, clinical discipline Substantial clinical study protocol experience, as lead author, required Experience leading and managing... teams while authoring regulatory documents with aggressive timelines Experience in regulatory submissions (clinical study...
or biomarker lead on cross-functional study teams, collaborating to address bioanalytical and biomarker-related challenges. Key..., and sample analysis; supporting regulated and non-regulated bioanalysis/biomarker analysis for toxicology and clinical studies...