- ThermoFisher Scientific (Wilmington, NC)
- …and supports business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic ... modules, etc. to ensure that the medical content is accurate and complete. ** Clinical Trial Support:** + Monitors all safety variables (AE, laboratory… more
- Cleveland Clinic (Cleveland, OH)
- …clinicians lack in-depth regulatory knowledge. You interact with physicians and investigators, clinical trial sponsors, clinical research team members, ... and analysis. + Interact with the Finance and Legal departments to facilitate clinical trial budget, site budget and contract execution. + Maintain professional… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Product Profiles, Clinical Development Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management ... supporting early or late development projects, reporting to the Associate Global Head or the Global Clinical ...of Full Development. + Provides medical oversight to the clinical trial program within their respective project… more
- AdventHealth (Orlando, FL)
- …than 32,000 inpatients and 125,000 outpatients each year **The role you'll contribute:** The Clinical Research Nurse RN/ Associate is a team member in the conduct ... of Phase I-IV industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols,...**The expertise and experiences you'll need to succeed:** + Associate 's of Nursing Required + Registered Nurse (RN) Current… more
- AbbVie (Waltham, MA)
- …analysis plans and reports + Leads integration of COA measurement strategy into clinical development programs through clinical trial program support (eg, ... / knowledge of the pharmaceutical industry (knowledge of regulatory/compliance frameworks) and clinical trial design + Knowledge of regulatory & HTA requirements… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments + Assists with and may author/review ... process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements. Considerable organizational awareness, including… more
- AbbVie (North Chicago, IL)
- …Completion of a subspecialty fellowship is desirable. + At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. + ... other program documents. + May oversee the work of Associate Medical and/or Scientific Directors, and of Clinical...a global scientific and business strategy. + Knowledge of clinical trial methodology, regulatory and compliance requirements… more
- AbbVie (San Francisco, CA)
- …scope of influence is within Development Operations, cross-functional colleagues who support clinical trial execution and the Development and Global Medical ... YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Clinical Operations Program Director is responsible to connect science and… more
- Danaher Corporation (New York, NY)
- …including managing people and cross-functional teams. + Demonstrated understanding of clinical trial design, GCP, and regulatory requirements (FDA, EMA, ... + Global clinical operations experience + Portfolio management tools and clinical trial management systems (CTMS). + Implementing DBS or Lean tools… more
- Cedars-Sinai (Los Angeles, CA)
- …and Safety Letters in accordance with local and federal guidelines + Assists with clinical trial budgets and patient research billing + Responsible for sample ... an organization known nationally for excellence in research!** The Clinical Research Associate I/CPT works under the...Academic / Research **Job Specialty** : Research Studies/ Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift** : Day… more