- Houston Methodist (Houston, TX)
- At Houston Methodist, the CTSA Program Project Manager ( Clinical and Translational Science Awards Program) position is responsible for the overall program ... Translational Science Alliance) registration and tracking system. The CTSA Program Project Manager will work closely with administrative counterparts at each of the… more
- Penn Medicine (Plainsboro, NJ)
- …Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn ... by registered pharmacists, certified pharmacy technicians, support staff, and four clinical pharmacists/full-time faculty members who are affiliated with the Ernest… more
- University of Southern California (San Diego, CA)
- …Project ManagerApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/ Clinical -Trial-Participant-Recruitment-Project- Manager ... Diego, California Clinical Trial Participant Recruitment Project Manager The USC Keck School of Medicine - Alzheimer's...manager for one or more of the various studies conducted at ATRI under the supervision of the… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …internal and external studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation ... office locations. Fully remote is not eligible._ The **Senior Clinical Study Lead** (CSL) is expected to...implements the operational strategic direction and guidance for respective clinical studies + Demonstrates expert knowledge and… more
- BeOne Medicines (Emeryville, CA)
- …+ Monitors resource utilization over the study life cycle + Ensures clinical studies at a project level are executed within endorsed time, quality, ... timelines and budget + Leads all aspects of assigned clinical study (ies) + Leads global cross-functional ...and tracks progress towards these + Ensures that the clinical studies are operationally feasible, oversees trial… more
- Abbott (Boston, MA)
- …+ Identify clinical opportunities through the use of analytics, time studies and/or field visits. + Address clinical opportunities through coaching or ... within Commercial to achieve region revenue growth goals and manage region's clinical specialists and resources. This position will identify and implement strategies… more
- Sanofi Group (Morristown, NJ)
- …formulating the nonclinical safety strategies, designing safety pharmacology and toxicology studies , authoring regulatory documents, being a member of an integrated ... Life Cycle Management/marketed products. + Write nonclinical summaries for clinical Investigator Brochures, INDs, CTAs and NDAs/BLAs, Pediatric Investigation Plans,… more
- Actalent (Smyrna, GA)
- …& Study Conduct: Recruit and enroll eligible subjects into clinical trials. Coordinate and schedule study -related procedures and appointments. Administer ... Key Job Responsibilities Study Start-Up & Regulatory Compliance: Facilitate study...Responsibilities Study Start-Up & Regulatory Compliance: Facilitate study initiation, including regulatory document collection and IRB submissions.… more
- OhioHealth (Columbus, OH)
- …the fundamentals of EBP and applies it to improve processes and clinical outcomes for specified patient populations. EBP fundamentals include completion of ... appraisal of the evidence/research articles, application of an EBP Methodology to clinical projects, etc. 15% Problem Solving 1. Facilitates and assists with solving… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. The ** Clinical Study Build Programmer - eCOA** is responsible for programming and testing ... flow, data standards, database programming, normalization and testing. The Clinical Study Build Programmer will collaborate with...collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager… more