Clinical Research EEG Monitoring Tech
|Position:||Clinical Research EEG Monitoring Tech|
|Experience Level:||Experienced (Non-Manager)|
The primary responsibility is to provide vigilant monitoring of recordings performed using Lifelines Neuro EEEG equipment. To ensure sites using our equipment are adequately trained in hardware and software requirements to meet protocol needs. To troubleshoot and provide technical support when necessary to ensure quality EEG data is obtained. Must be experienced with navigating technical challenges along with solving complex problems with decisive critical thinking skills.
Complete monitoring of recordings, per contract obligations both remote and on-Site
Continuously monitors neurodiagnostic studies performed by research sites, based on the protocol set for each study.
Complete initial study review accurately according to study protocol requirements.
Complete accurate independent data reports developed for each study protocol.
Supports the start-up, monitoring, and closeout phases of assigned clinical trials.
Ability to troubleshoot basic neurodiagnostic technical issues, document, and escalate as required. Including software, hardware, connections, uploads, and basic IT functions.
Provide basic technical support via remote access software, such as Team Viewer, Go to Assist, telephone, and/or email. *
Has the capability to identify biological and non-biological artifact and find ways to eliminate and correct sources, and communicate with remote sites how to correct errors.
Monitor transfer of data collected during EEG recording and after patient disconnect.
Provide remote training and assist sites with successful studies and collection of data required from the study protocol.
Must accurately document all data gathered during studies. *
Adhere to SOP’s, and work instructions developed for each study protocol.
Minimum of 3 years’ experience in initiation, conduct, and monitoring of EEG recordings
Must hold at least one registry in the following fields: R.EEG T., CNIM, CLTM or a combination of the registries, and maintain registrations.
Minimum 1-year experience assisting with clinical research trials to include compliance, data collection, and data management
Extensive knowledge of HIPAA, ICH-GCP, 21 CFR 11, GDRP, and other applicable regulations
Strong interpersonal skills with the ability to respond professionally with clients and internal personnel from international cultures whose primary language may not be English
Attention to detail
Preferred: Bachelor’s degree from an accredited four-year university.
Must be willing to travel when requested. Remote work location.