- Sumitomo Pharma (St. Paul, MN)
- …International Council for Harmonization E6(R2). + Fundamental knowledge of the conduct of clinical trials is preferred. + Strong focus on teamwork, attention to ... our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be...ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure… more
- Georgetown Univerisity (Washington, DC)
- …Diseases Clinical Trials Unit will work with and assist the Clinical Research Coordinator, Regulatory Specialist , and Clinical Trial ... the Clinical Research Coordinator, Regulatory Specialist , and Clinical Trial Manager...7 years of experience working with clinical trials and supporting a clinical trial… more
- Stony Brook University (Stony Brook, NY)
- Research Nurse - Cancer Clinical Trials **Position Summary** The **Research Nurse** for the Cancer Center Clinical Trials Department is responsible for ... AE logs, con meds, etc.) in source material, and enter necessary information into Clinical Trial Management System (CTMS). + Assist with organizing, and attend… more
- University of Utah (Salt Lake City, UT)
- …Quality Oversight** + Conduct routine internal audits and targeted reviews of clinical trial documentation including regulatory binders, subject binders ... research study teams, and clinical teams, the QA Specialist ensures regulatory compliance, operational efficiency, and consistently high standards… more
- Boehringer Ingelheim (Ridgefield, CT)
- … programs across Therapeutic areas, ie, Clinical Associates (CAs), Clinical Trial Operations Specialist (CTOS), Regulatory Start Up Specialist ... for forecasting and providing oversight of resources supporting US Clinical Trial Managers (CTMs)and managing the Site...trials based on input from 3rd party vendor(s), Regulatory Start Up Specialists (RSUS), trial team,… more
- Weill Cornell Medical College (New York, NY)
- …role when Hired for NYC Offices **Position Summary** Under general direction, oversees the regulatory aspects of clinical trials from start-up through study ... Title: Regulatory Specialist -CCTO Location: Lower East Side...visits, regulatory monitoring visits, and assists with clinical trial audits or inspections. + Maintains… more
- Edwards Lifesciences (Kansas City, KS)
- …clinical trial /study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements + Develop and deliver technical training ... make an impact:** + Field monitoring of studies and data collection for clinical trials , assess all data documentation, reports, records, transcripts, exam… more
- J&J Family of Companies (Danvers, MA)
- …testing, and site closeouts. As a subject matter expert on clinical trial protocol and technologies, the Field Research Specialist acts a liaison between ... clinical background in procedural areas. The Field Research Specialist is a dual-role position that combines field-based ...call, bedside case coverage for multiple clinical trials and clinical trial sites.… more
- ICON Clinical Research (NJ)
- Clinical Study Specialist (office based) ICON...plan + Monitors and updates investigator/site status for the trial , and supports with clinical trial ... registry postings + Performs scheduled reconciliations of study Trial Master File (TMF) with clinical study lead guidance + Ensures scheduled reports are… more
- Abbott (Abbott Park, IL)
- …colleagues serve people in more than 160 countries. **Job Title** **Principal Field Clinical Specialist ** **Working at Abbott** At Abbott, you can do work ... **The Opportunity** We currently have an opportunity available for a **Principal Field Clinical Specialist ** to join our **Vascular** division. **This is a fully… more