- Insight Global (Beachwood, OH)
- …study activities including site selection, investigator engagement, initiation, monitoring, and study closeout. o Ensure studies are conducted in compliance ... Strategy & Protocol Development o Lead the development of IRB and clinical study protocols in alignment with company objectives. o Collaborate with surgeons and… more
- ThermoFisher Scientific (Greenville, NC)
- …+ Provides medical consultation to team members and answer all study related medical questions. Communicates clearly with associates and clients, maintaining ... followed appropriately. + Provides therapeutic training and protocol training on assigned studies , as requested. + Assists in writing (interpretation of safety and… more
- SUNY Upstate Medical University (Syracuse, NY)
- …human through phase 3 trials. The role will be expected to manage 2-3 studies simultaneously. The will ensure compliance with FDA guidelines and follow GCP for all ... managed studies . The CRA I will interact daily with clinicians,...the candidate needs the ability to communicate directly with study volunteers, collecting detailed clinical information and communicating that… more
- Charles River Laboratories (Cleveland, OH)
- …and issues that are related to formulations and chemicals used on study . Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role ... as labeling and solution preparations + Assist with maintaining study specific inventory of consumables with oversight + Write...the operational area + Assist in execution of routine studies with oversight + Assist in execution of assay… more
- Vanderbilt University Medical Center (Nashville, TN)
- …The applicant will be primarily responsible for coordinating clinical research studies in patients with frontotemporal Lobar Degeneration (FTLD), as well as ... disease. This position will specifically focus on investigator initiated, longitudinal studies in the Darby lab. Responsibilities will include: 1.) Coordinating the… more
- Baylor Scott & White Health (Plano, TX)
- …in compliance with regulatory laws and institutional guidelines. May assist in complex studies with direction but does not have overall responsibility for these ... studies . + Communicates with research participants via phone calls,...in maintaining regulatory binders. + Assists research physicians with study proposal development and helps to ensure that appropriate… more
- University of North Carolina- Chapel Hill (Chapel Hill, NC)
- …on all research and stakeholder engagement activities related to these externally funded 36-month studies . The first study will develop and evaluate a novel CGM ... track CGM prescribing patterns over 6 months after completion of the study to evaluate clinical and patient-reported outcomes, and analyze provider documentation to… more
- Mount Sinai Health System (New York, NY)
- …the medical order. Follows sleep center protocols related to the sleep study . 4. Upon patient arrival, verifies identification, collects documents and obtains ... consent for the study . 5. Explains the procedure and orients the patient...Latency Test (MSLT), Maintenance of Wakefulness Test (MWT), parasomnia studies , PAP and oxygen titration, etc.] to ensure collection… more
- AbbVie (Irvine, CA)
- …and creatively apply methodology and analytical skills to bring resolute answers through novel study design. The position may be filled at either the Director I or ... in Irvine, CA. Key Responsibilities + Define objective and develop study design scenarios/options to support novel non-interventional and interventional studies… more
- Mount Sinai Health System (New York, NY)
- …the medical order. Follows sleep center protocols related to the sleep study . 4.Upon patient arrival, verifies identification, collects documents and obtains consent ... for the study . 5.Explains the procedure and orients the patient for...Latency Test (MSLT), Maintenance of Wakefulness Test (MWT), parasomnia studies , PAP and oxygen titration, etc.] to ensure collection… more