• Serves as a source of medical expertise for clinical project teams • Provides input to decisions that have medical, scientific, and future marketing implications • Provides medical input into the design, planning, initiation and completion of clinical trials • Responsible for the preparation of the medical components of study protocols and IND and other regulatory submissions • Serves as the medical monitor for the successful conduct, integrity, and safety of patients in our clinical trials • Partner with Research, Regulatory Affairs, Medical Affairs, Biometrics, Clinical Operations, Safety, Quality Assurance, Product Development, Business Development, and Management to formulate and implement comprehensive clinical trial plans • Establishes communications and relationships with prominent clinical investigators in the area of cardiovascular disease • Attends appropriate scientific meetings to maintain awareness of research activities and represents a project and/or Company at such external events • Applies the strategic intent of the Company when working with regulatory bodies such as FDA, and with key opinion leaders • Performs product safety medical reviews for assigned investigational drugs • Ensures an appropriate level of customer service to internal and external customers

• Provides medical oversight of clinical trials • Attends and presents at investigator and sponsor meetings • Provides medical consultation to clients and project team members • Manages signal detection activities and medically reviews adverse events • Monitors safety variables of clinical studies

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description Work 100% remotely caring for dementia patients—with time, autonomy, and support. - Role: Neurologist (Dementia & Cognitive Disorders) - Location/Type: Anywhere in the U.S. • 100% Remote - Pay: $62,400–$124,000 Part Time - Work Type: Part-time 1099 (10-20 hours per week) - Schedule: Flexible, 4-hour half-day blocks Thoughtful dementia care. No call. No commute. No rushed visits. What you’ll do - Evaluate patients with ADRD (Alzheimer’s and related disorders) - Manage dementia, cognitive decline, and behavioral symptoms - Review and interpret neuroimaging - Deliver care using clear, established clinical protocols - Collaborate with and supervise APPs as the team grows - Join case reviews and care coordination - Support clinical leadership as the organization scales Qualifications - Board certified neurologist (ABPN) - Active U.S. medical license (any state) - Dementia experience or strong willingness to learn protocols - Excellent bedside manner and patient communication - Comfortable practicing independently in a remote setting Requirements - UCNS Board Certification in Behavioral Neurology (nice to have) - General neurology background with dementia-heavy panels (nice to have) - Neuro-oncology, geriatrics, palliative care, or PMHNP collaboration (nice to have) - Multi-state licensure (nice to have) Benefits - Pay: $62,400–$124,000 (part-time) - Part-time option: 1099, per-visit model with specialty premium - Equity: Available for full-time hires - Bonus: RVU-based (salaried roles) - CME: Uncapped allowance (review-based) - Licensing support, malpractice, PTO Impact & Growth - Your work improves care for patients and families navigating dementia. - Early hires grow into regional and national medical leadership roles. - You like autonomy, ownership, and meaningful patient relationships. At Urrly, fairness matters. We use AI to review every application against the same clear requirements for the role. This means every candidate is evaluated on job-related factors like skills, certifications, and experience—not on personal attributes such as gender, race, age, or background. Our goal is to create a more objective, consistent, and equal opportunity hiring process for all applicants. Apply Today to work remotely in a role open to full-time or part-time 1099 neurologists—real impact, flexible schedule, no call.

• Provide medical monitoring for assigned projects • Function as medical representative on the project team • Provide medical consultation to clients • Review individual adverse experience reports • Provide reports to FDA or other regulatory agencies • Review data listings of safety data • Support preparation of clinical protocols