- AbbVie (North Chicago, IL)
- …aides in the planning, conduct and reporting of non-GLP and GLP toxicology studies , acting to support the Study Director and regulatory infrastructure. MAJOR ... SCOPE: + Responsible for key tasks in the set-up and conduct of nonclinical studies + Support the Study Director, acting as a designee for some tasks + Study … more
- University of Utah (Salt Lake City, UT)
- …conduct quality control activities (field/ study visits, data queries) 15. Determine study visit and site/clinic work flows for studies /protocols 16. Work ... & Athletic Training is seeking an individual to support clinical research studies evaluating various rehabilitation interventions for persons with chronic pain that… more
- Pfizer (Pearl River, NY)
- …development program. This role may serve as a clinical lead for one or more studies within a clinical program and works closely with the global clinical program lead ... will be set within a matrix team in executing studies , performing medical monitoring, supporting regulatory interaction, and taking...regulatory interaction, and taking on a leadership role in study teams for many of the clinical deliverables. The… more
- Actalent (Cincinnati, OH)
- …logistics. + Request study -specific equipment and instrumentation. + Collaborate with study coordinator to request and schedule studies to meet project ... We are seeking a dedicated Preclinical Research Assistant to support the Study Director and Preclinical Sponsor Representatives in the preparation and conduct of… more
- University of Utah (Salt Lake City, UT)
- …Monday through Friday, 8:00am - 5:00pm. Some variance in shift times may occur per study needs. On-call for holidays and as needed to provide study coverage. ... projects ranging from internal chart reviews to large, industry and federally funded studies . This individual will work closely with our investigators, study … more
- Johns Hopkins University (Baltimore, MD)
- …and scientific implementation of clinical research protocols for complex and/or multiple clinical studies . As part of a study team, collaborates with faculty, ... develops protocol, develops SOP, and oversees study -related activities for one or more studies ....oversees study -related activities for one or more studies . **Specific Duties & Responsibilities** _Project Management_ _Pre-study_ +… more
- University of Michigan (Ann Arbor, MI)
- …We are seeking a responsible, motivated, individual who will independently provide study coordination for simple and moderately complex clinical research studies ... theMichigan Medicine CRC Career Ladder (https://medresearch.umich.edu/office-research/about-office-research/our-units/clinical-trials-support-office/ study -coordinator-support/clinical-research-coordinator-career-ladder) is required. This position… more
- University of Miami (Miami, FL)
- …the implementation of behavioral, community-based, and cancer prevention research studies within the Behavioral Community-Based Research Shared Resource (BCSR). This ... and compliance monitoring to support the smooth operation of multiple BCSR studies . This role requires strong attention to detail, interpersonal skills, and a… more
- Rush University Medical Center (Chicago, IL)
- …- Manages multiple studies with little oversight; sets priorities and keeps study tasks on track. * Problem-Solving & Critical Thinking - Solves complex problems ... III (CRC III) independently manages the full scope of clinical research study execution for complex, multi-site, or longitudinal protocols. This role is responsible… more
- University of Pennsylvania (Philadelphia, PA)
- …changes to procedures as needed and monitor results. Responsible for study coordination for investigator-initiated studies , multi-center research studies ... subject enrollment, collection and storage of biological samples and related study documents, and collection of clinical data. Assist with Institutional Review… more