- J&J Family of Companies (Irvine, CA)
- …to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones; + Oversees/executes feasibility, selection, ... (eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports, ); + Supports applicable trial registration (eg… more
- University of Michigan (Ann Arbor, MI)
- …Demonstrates the ability to anticipate and mitigate the potential for protocol non- compliance . + Describes protocol structure and explains how to interpret study ... requirements to ensure study compliance . + Demonstrates accurate implementation of protocol procedures. +...University and Federal guidelines in order to assist with Investigator Initiated studies. + Collaborates with MIAP for INDs… more
- J&J Family of Companies (Irvine, CA)
- …Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for JJMT Electrophysiology + ... study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports), ensure registration on www.clinicaltrials.gov from… more
- Johns Hopkins University (Baltimore, MD)
- Reporting to the Principal Investigator (s), we are seeking a **_Sr. Research Nurse_** , to Lead Research Nurse. This position is responsible for the coordination and ... of protocol by pharmacy for review & input as appropriate. + Assures compliance with local & national regulatory standards. + Collaborates with study team and… more
- J&J Family of Companies (Irvine, CA)
- …to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones. + Oversees/executes feasibility, selection, ... (eg study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports); + Ensures applicable trial registration (eg on… more
- Sumitomo Pharma (Topeka, KS)
- …+ Assesses and communicates regulatory requirements ensuring activities are in compliance with applicable regulations and guidelines + Leads documentation of ... CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contributes to content as needed… more
- J&J Family of Companies (Irvine, CA)
- …Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Biosense Webster; + ... study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports), ensure registration on www.clinicaltrials.gov from… more
- State of Arkansas (Little Rock, AR)
- …Job Summary: Hiring Official: LaQuisha Shead This position is an INVESTIGATOR . Travel is required for this position. PREFERRED QUALIFICATIONS: *Experience managing ... Summary: Review Incident and Accident claims as assigned by the lead investigator Perform a thorough investigation in person/virtual of all sources. These… more
- Alaka'ina Foundation Family of Companies (Camp Lejeune, NC)
- …or counter to society's mandates and suggests potential corrective measures to the investigator and CIDH for remediation. Report serious non- compliance issues to ... is evaluated by observation and outcomes for effectiveness of operations and compliance with medical requirements and professional standards in terms of quality and… more
- Kelly Services (Irvine, CA)
- …R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones + Supports the clinical study team ... study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports), and applicable trial registration on… more