- Rush University Medical Center (Chicago, IL)
- …knowledge of current NIH and/or FDA regulations and guidelines related to clinical research . * Strong project management skills including ability to ... institutional, local, state and federal guidelines and regulations related to clinical research . * May collect, process and ship potentially biohazardous… more
- Rush University Medical Center (Chicago, IL)
- …order to prepare a billing plan for all medical procedures and services required in a clinical research project . * Review clinical research protocols ... in the growing efforts to conduct prospective Medicare Coverage Analysis for all clinical research studies. Exemplifies the Rush mission, vision and values and… more
- Rush University Medical Center (Chicago, IL)
- …documents to prepare a billing plan for all medical procedures and services required in a clinical research project . * Review clinical research ... in the growing efforts to conduct prospective Medicare Coverage Analysis for all clinical research studies. Exemplifies the Rush mission, vision and values and… more
- Rush University Medical Center (Chicago, IL)
- …Good Documentation Practices. * Demonstrated knowledge of current NIH and/or FDA regulations and guidelines related to clinical research . * Ability to meet ... deadlines and help coordinate multiple aspects of the ongoing project . * Strong organizational and problem-solving skills. * Detail...and federal guidelines and regulations related to clinical research . * May collect, process and… more
- American Heart Association (Chicago, IL)
- …clinical datasets (including real world data) from multiple American Heart Association clinical trials, research studies and registries as well as other large ... data dictionaries. + Collaborate with subject matter experts in clinical data and research , and external entities...Case Report Forms, Surveys, EHR queries and other data project documentation process. + Develop and implement guidelines… more
- Capgemini (Chicago, IL)
- …a Vice President and Project Manager in the pharmaceutical, biotechnology, or clinical research industry, with a strong background in Clinical ... (CTMS), and related tools. + Comprehensive understanding of clinical research processes, biostatistical environment and regulatory guidelines (eg, ICH-GCP)… more
- Elevance Health (Chicago, IL)
- …strongly preferred. + Clinical or therapeutic area knowledge, familiarity with clinical practice guidelines , and/or understanding of the US health care ... **Researcher Senior - Safety and Epidemiology Research ** **Location:** This position will work a hybrid model (remote and in office one day per week). Ideal… more
- IQVIA (Chicago, IL)
- …IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in ... deliverables. Perform role of Data Team Lead (DTL). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines , SOPs, policies, and, where… more
- IQVIA (Chicago, IL)
- …IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in ... a specific CDM task (eg, Subject Matter Expert (SME). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines , SOPs, policies, and, where… more
- IQVIA (Chicago, IL)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice (GCP) and ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- AbbVie (Chicago, IL)
- …Certification or Lean Six Sigma Green Belt desired. + Must have 6+ years of pharma / clinical research / data management / health care experience or 8+ years of ... + Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines , AbbVie Standard Operating Procedures… more
- AbbVie (Chicago, IL)
- …PRISMA guidelines . + Advanced understanding of drug development, clinical research , study designs, biostatistics, pharmacology, regulatory requirements, and ... in assimilating and analyzing complex data + Extensive experience writing, editing clinical documents following guidelines and regulations, such as ICH … more