- University of Miami (Miami, FL)
- …alternative language, as required. + Communicates (telephone, email, meetings) with principal investigator and key senior leadership authors as necessary to ... understanding of the target audience. This job also assists the Principal Investigator (PI) with the development and/or completion of scientific documents, which… more
- Cedars-Sinai (Los Angeles, CA)
- …projects and proposals. + Assists in the preparation of grant proposals of Senior Investigators . + Compiles, analyzes, interprets, and summarizes data. + May ... cooperation with Piotr Slomka, PhD, Director, Innovation in Imaging and Principal Investigator , as part of a medical imaging and artificial intelligence research… more
- Mayo Clinic (Rochester, MN)
- …position. The Career Scientist position is a tenure-equivalent position for a Principal Investigator to develop and run an independent research program with a joint ... of Surgery and Artificial Intelligence/Informatics. The primary focus of the Investigator 's research endeavors should be broadly within the field of artificial… more
- MD Anderson Cancer Center (Houston, TX)
- …visits and termination. *CLINICAL TRIALS COORDINATION* * Consults with principal investigator and other department personnel verbally, in handwritten notes or via ... keyboard on computer regarding ongoing studies; requires ability to gather information and determine the appropriate information to report. * Participates in protocol site initiation/logistics meetings and attends departmental or institutional research… more
- Insight Global (Beachwood, OH)
- …& Oversight o Oversee clinical study activities including site selection, investigator engagement, initiation, monitoring, and study closeout. o Ensure studies are ... conducted in compliance with approved protocols, regulatory standards, and timelines. o Perform site visits, oversee test article reconciliation and disposition, and maintain accurate documentation. - Data Integrity & Reporting o Ensure the accurate… more
- Medtronic (Boston, MA)
- …knowledge and experience + Knowledge of physical security technology + Experienced investigator and report writer + Ability to successfully navigate in a complex ... matrixed organization + Strong communicator who displays exceptional presentation and persuasion skills (verbal and in writing) with complex issues + Ability to think both strategically as well as operationally + Ability to maintain professional demeanor under… more
- Mayo Clinic (Rochester, MN)
- …some assignments independently as discussed and approved by Principal Investigator . **Qualifications** Requires bachelor's degree in biology, chemistry, or other ... relevant science with 4 years of research laboratory experience (5 years preferred). Master's degree in biology, chemistry, or other relevant science preferred. Must exhibit a solid understanding of lab techniques, equipment, and safety. Must have the ability… more
- Merck (Rahway, NJ)
- …trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update ... reports, study close out activities). + Leads team for timeline management, risk identification and mitigation, issue resolution. + May facilitate and collaborate with key internal/external stakeholders (eg, study team, country teams, vendors, committees) in… more
- AbbVie (North Chicago, IL)
- …population PK reports, exposure-response analyses reports, relevant section of investigator brochures, common technical documents, white papers, and other similar ... documents. + Conduct data analyses including non-compartmental analyses, modeling and simulation, literature data analyses. + Participate and present at various departmental and cross functional teams such as study teams, clinical pharmacology and… more
- Merck (Austin, TX)
- …+ Worldwide marketing applications + Clinical study protocols and reports + Investigator brochures + Local registration study protocols for secondary markets + ... Represent Global Regulatory Affairs on internal committees (eg, DRC, ADT/PDT, EDT, LEAD) to provide strategic regulatory input and approvals. + Conduct initial content review and approval for IND/CSA submissions to enable clinical trial initiation. +… more