- OhioHealth (Columbus, OH)
- …out the research in an efficient and timely manner. Assists with protocol feasibility, resource requirements and study planning activities including leading internal ... training to implement the protocol and avoid deviations. Assists with recruitment procedures for...visits by monitors or Sponsor representatives. Participates in in-house protocol meetings to review study-related procedures, staffing and visit… more
- Bristol Myers Squibb (Princeton, NJ)
- …(matrix leadership) + Co-Leads study team meetings in partnership with GDO protocol manager; and collaborate with cross functional study team members + May ... Responsibilities** + Maintain a thorough understanding of assigned protocols and protocol requirements; educate supporting team members + Plan and lead the… more
- University of Miami (Miami, FL)
- …the compilation, registration and submission of data, monitoring compliance with the protocol , adherence to SOPs, and all applicable regulations and guidelines. CORE ... are documented and meet both internal and external regulations in accordance with protocol guidelines.8. Maintains logs (ie TAS submissions, Velos etc.) in a timely… more
- Boehringer Ingelheim (St. Joseph, MO)
- …ensure that the studies are conducted in compliance with the current approved protocol , GCP/ VICH requirements, FDA/CVM Regulations, and BI SOPs. The incumbent is ... + Collaborates with the Clinical Scientist and Study/Trial team in protocol development, CRF design, writing amendments, creating site-training materials, final… more
- Logan Health (Whitefish, MT)
- …sterile supplies and equipment for procedures. + Performs proper hand washing protocol , donning of sterile attire, and begin preparations for the surgical procedure ... for the patient by maintaining the integrity of the sterile field per department protocol . + Evaluates all instrumentation and technical equipment to assure it is in… more
- Johns Hopkins University (Baltimore, MD)
- …with PI and study team to ensure operational feasibility of proposed protocol /study design. + Develop standard operating procedures and data collection forms from ... protocol (s). + Develop consent form(s) for clinical trials based on protocol (s). + Prepare materials for submission to IRB and follow-up on regulatory issues. +… more
- Teleflex (Minneapolis, MN)
- …teams to support all phases of a clinical study including protocol , CRF, and monitoring plan development, essential document management, contract execution, ... Interim, and Close-Out monitoring visits to ensure adherence to monitoring plan, protocol , and regulations. * Train site personnel regarding the protocol … more
- University of Rochester (Rochester, NY)
- …by phone, email, and other electronic interfaces. + Follows prescribed protocol and Standard Operating Procedures to schedule patient appointments, resolve patient ... + During the call, makes independent decisions to act outside of the protocol to transfer, refer or resolve emergent situations. + Assesses the urgency of… more
- IQVIA (Troy, NY)
- …practice to senior staff. **Support Study Conduct By:** + Reviewing the study protocol , case report form (CRF), other study documents, and electronic data capture ... and documents. + Planning logistical activity for procedures as per protocol . + Generating volunteer instructions. + Identifying and obtaining required supplies… more
- Stony Brook University (Stony Brook, NY)
- …Nurse** for the Cancer Center Clinical Trials Department is responsible for the Protocol Management reviews for active and potential protocols. This, in large part, ... includes the determination of patient eligibility for protocol participation by way of chart review, data collection and patient evaluation/assessment… more