Ethan Solomon Email & Phone Number

Dublin, California, United States

San Francisco Bay Area (Remote)

• Responsible for collaborating with assigned research sites in the GAP-Network on recruitment and process optimization for specific Alzheimer’s and Parkinson’s disease clinical trials • Provide strategic input to clinical sites on effective recruitment, outreach and optimization strategies• Work closely with pharmaceutical and biotech companies, CROs and vendors in a collaborative, professional and highly effective manner. • Navigate and possess an in-depth understanding of complicated clinical trial protocols • Facilitate sharing across GAP-Network research sites with regards to learnings and best practices by creating presentations or tools, speaking at conferences and/or webinars, and fielding requests for assistance and information on effective strategies for recruitment and optimization. • Provide input and assistance as needed with project proposals, reports, manuals, and other documentation as needed.• Assist in development and execution of marketing strategies, social media engagements, event or program management, and community outreach events• Accountable for writing site visit reports for the study sponsor and/or contract research organizations (CROs) and provide consistent and immediate support to assigned research sites in order to help maximize their productivity

San Francisco Bay Area

• Identify, engage, develop and manage field-based relationships with medical and scientific stakeholders including key HCPs and medical decision makers within 3 of the 5 largest IDNs in the nation• Collect and communicate insights from external medical and scientific stakeholders in the field to identify gaps in clinical evidence and education• Demonstrate credibility of current clinical interventions and protocols through presentation of clinical data and real world evidence• Develop and implement field based medical education programs and scientific events for KOLs and healthcare professionals• Monitor evidence generation programs within IDNs and liaise when necessary within Medical Affairs• Provide scientific expertise and education to KOLs, HCPs, National/Strategic account teams and internal sales force• Identify, initiate and execute scientific activities to support novel medical claims

San Diego, California

• Identify, establish and manage relationships with Key Opinion Leaders (KOLs) & HCPs in therapeutic areas of Neurology and Aging Sciences throughout Pacific Northwest territory• Provide scientific expertise & education to KOLs, HCPs and key study personnel for Phase III therapeutic trial• Collect and communicate insights from external medical and scientific stakeholders in the field to contribute to the update of study protocol, procedures and scientific data• Collaborate and assist with multi-disciplinarian team from recruitment, regulatory affairs, and finance to facilitate study progress• Review, evaluate and report clinical test results and adverse events to ensure participant safety, data quality and standardization• Analyze scientific databases for accuracy, completeness and reliability. Design and implement corrective procedures when necessary • Oversee and coordinate all aspects of site qualification, initiation and activation• Independently conduct audits of assigned study sites to ensure all necessary data has been collected and documented accurately

Stanford, Ca

•Oversee and monitor multiple high visibility Phase III and Phase I trials•Develop project schedules, targets, measurements, and accountabilities•Audit operations, including laboratory procedures, to ensure compliance with applicable regulations •Provide leadership in determining, recommending and implementing improvements to processes to ensure safety and efficacy of clinical trials •Solely responsible for subject recruitment and meeting study enrollment goals•Oversee data management/quality assurance for multiple clinical trials •Develop and manage systems to organize, collect, report, and monitor data collection•Monitor and create regulatory documentation and respond to internal and external queries•Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials•Manage resources within study budget, working with senior staff and principal investigators, identifying standard of care versus study procedures•Supervise, train, and mentor junior research associates•Track patient and study specific milestones, and invoice sponsors according to study contract•Ensure and monitor regulatory compliance by regularly inspecting and editing study document

Walnut Creek, Ca

• Assist in coordinating Phase 3 sponsor-initiated therapeutic trials and national clinical research projects studying memory loss, aging and other neurodegenerative diseases• Coordinate with principal investigators and sponsors to ensure regulatory compliance and monitor protocol procedures• Create, maintain and analyze datasets and databases for various clinical trials and research studies• Prepare and analyze test results and behavioral assessments for Neuropsychologists and Neurologists to determine protocol eligibility• Collect and aggregate longitudinal data for all neuropsychological tests administered at East Bay Site• Develop quality control procedures to maintain standardized methods consistent with protocols across psychometrists• Develop versatile rapport building skills to communicate and assist patients with cognitive compromise and their respective caregivers• Extensive experience administering and scoring various neuropsychological and behavioral tests• Trained and supervised student research assistants• Conferred numerous Employee Recognition Awards • Solely responsible for IT management and support at Easy Bay Site

San Diego, California

• Collect and analyze data in a high visibility clinical study researching memory in elderly individuals at risk for Alzheimer’s disease and other genetically inherited neurological disorders• Collaborate with principal investigator and research staff to ensure compliance with protocol requirements• Administer and score battery of neuropsychological and psychophysical tests• Trained in all aspects of electrophysiological data collection

San Diego, California

• Create, conduct and assisted research protocols investigating the effects of aging on cognitive functioning in subjects at risk for Alzheimer’s disease and other genetically inherited neurological disorders• Create and update data management systems and data quality controls measures• Collaborate with principal investigator and research staff to ensure compliance with protocol requirements• Administer and analyze Neuropsychological, behavioral and psychophysical tests• Perform literature reviews to keep abreast of current trends within Aging sciences• Obtained certification in both EEG and fMRI research methodologies

San Diego, California

• Create teaching material and informational presentations for classes of up to 400 students• Organize and present weekly academic advising sessions for undergraduate students interested in pursuing careers in research• Conduct class lectures in professors’ absence• Selected as judge for numerous undergraduate research symposiums• Selected by graduate school faculty to be a member of the faculty selection committee• Generate lectures and supplementary material for upper-division Neuroscience classes: Developmental Psychopathology, Neuropsychology, Drugs & Behavior, Psychology of Personality, Statistical Methods, Behavioral Neuroscience, and Social Psychology

Master Of Arts (Ma), Behavioral And Cognitive Neuroscience (Psychology)

Activities and Societies: Judge for Undergraduate Research Symposium, Member of Student/Faculty Selection Committee, Exemplary Academic.

Bachelor Of Science (Bs), Biological Sciences/Minor In Cognitive Science

Undergraduate research assistant in Cognitive Science projects investigating cognitive functioning and how the brain encodes, processes.