Sr. Clinical Research Asst.

4 weeks ago

Belmont, United States Partners Healthcare System Full time

The Laboratory for Functional Neuroimaging & Bioinformatics (FNIBI) at McLean Hospital, Belmont, MA is hiring a full-time Sr. Clinical Research Assistant. The FNIBI conducts research to understand the nature and underlying biology of mental and neurological illnesses. One of our goals is to develop naturalistic approaches for dynamic assessment of verbal and non-verbal communication in real-world settings, specifically tailored for individuals with a mental or cognitive impairment. In this research, we use behavioral, multimodal neurophysiological, and computational methods to characterize behavior at multiple levels, and identify phenotypes of communication malfunction.

Working under the supervision of Dr. Einat Liebenthal (Principal Investigator), the Sr. Clinical Research Assistant will work on a project titled Naturalistic Neuroimaging for Presurgical Language Mapping, funded by the NIH/NIDCD. As part of this project, language functions associated with movie-watching are evaluated in individuals with stroke-induced aphasia and healthy controls, using behavioral, eye-tracking, and neuroimaging methods.

A two-year commitment from the candidate is requested. The position offers an excellent opportunity for an individual in a doctoral program, particularly in the areas of cognitive neuroscience or speech language pathology. This position provides exposure to a multi-disciplinary team of researchers and clinicians, as well as opportunities to attend academic conferences.

Principal Duties and Responsibilities

* Collects and organizes patient data
* Maintains records and databases
* Uses software programs to generate graphs and reports
* Recruiting patients for clinical trials, conducts phone interviews and schedules patients for visits.
* Obtains patient study data from medical records, physicians, etc.
* Conducts library searches
* Performs administrative support duties as required
* Verifies accuracy of study forms
* Updates study forms per protocol
* Prepares data for analysis and data entry
* Assists with formal audits of data
* Documents patient visits and procedures
* Assists with regulatory binders and QA/QC procedures.
* Assists with interviewing study subjects
* Administers and scores questionnaires
* Provides basic explanation of study and in some cases obtains informed consent from subjects
* Performs study procedures such as phlebotomy
* Assists with study regulatory submissions
* Writes consent forms
* Verifies subject inclusion/exclusion criteria
* Assists with determining suitability of study subjects
* Maintains research data, patient files, regulatory binders and study databases
* Performs data analysis and QA/QC data checks
* Organizes and interprets data
* Has input into recruitment strategies
* Acts as study resource for patient and family
* Monitors and evaluates lab and procedure data
* Administers/scores/evaluates study questionnaires
* May contribute to protocol recommendations
* Assists with preparation for annual review
* Assists PI to prepare complete study reports & presentations
* Independently determines suitability of study subjects
* Develops and implements recruitment strategies
* Partipates in the design of research methodology
* Plans, performs and designs statistical analyses
* Recommends protocol changes and writes protocols and contributes to manuscripts.
* * Independently performs specialized projects
* Education - Bachelor's Degree required master's degree preferred
* Experience: Minimum 3-years related post bachelor's degree experience required

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