Clinical Research Coordinator I

Epia Neuro; Alameda (CA); Hybrid; USD 34,000 - 41,000; Part time

Job summary

Epia Neuro is seeking a Clinical Research Coordinator I to support the day-to-day execution of a user study evaluating a wearable robotic device for stroke-related motor impairment. You will assist study documentation, participant scheduling, and in-visit support, collaborating closely with the study and engineering teams.

Responsibilities include drafting SOPs, assisting with enrollment, coordinating visits, and ensuring data integrity per GCP.

Qualifications

• Bachelor's degree in health sciences, biology, kinesiology, psychology, or a related field.
• Familiarity with GCP, IRB protocols, or clinical study documentation is a plus, but not required.

Responsibilities

• Draft and maintain SOPs and IRB-ready study documentation for visit workflows.
• Support enrollment and screening with logs and case report forms.
• Schedule visits and manage the study calendar with the team.
• Take anthropometric measurements and 3D scans for device sizing.
• Greet participants, orient them to the visit, and guide study activities.
• Manage in-visit data collection and study records per protocol.

Skills

Communication

Organization

Scheduling

SOP Writing

Participant Interaction

Education

Bachelor's degree (health sciences/biology/kinesiology/psychology)

Tools

GCP familiarity

Job description

About Us

Epia Neuro is a neural technology company developing intent-driven systems designed to restore function and independence for people living with neurological conditions. Its platform integrates implantable neural interfaces, adaptive algorithms, and assistive devices to translate neural intent into real-world action. The company’s initial focus is stroke-related motor impairment, with expansion in cognitive decline and other neurological disorders, focusing on long-term solutions for the growing aging population.

How We Work

• We are intentional. We prioritize and are thoughtful about how we use others' time.
• We care for others. We prioritize safety both for patients and one another.
• We own outcomes, not just tasks. Our work demands the highest standards because it impacts real patients and real lives.
• Humility is a strength. We are honest about what we know and what we don't know. Getting it right matters more than being right.

The Role

We're looking for a Clinical Research Coordinator I to support the day-to-day execution of our user study evaluating a wearable robotic device for people with stroke-related motor impairment. You'll support study documentation, participant scheduling, and in-visit support, working closely with the study and engineering team.

Key Responsibilities

• Draft and maintain Standard Operating Procedures (SOPs) and IRB-ready study documentation for study visit workflows, device fitting, and sizing/scanning procedures.
• Support participant enrollment and screening, including maintaining enrollment logs and case report forms in compliance with GCP.
• Schedule study visits with participants and manage the study calendar, coordinating with the study team and clinical site as needed.
• Take anthropometric measurements and 3D scans of participants to inform device sizing and fit, per protocol.
• Serve as the participant's day-of point of contact — greeting them on arrival, orienting them to the visit, and guiding them through study activities.
• Support in-visit data collection and manage study records (visit logs, case report forms, data quality checks) per protocol and data-handling procedures.

Qualifications

• Bachelor's degree in health sciences, biology, kinesiology, psychology, or a related field.
• Familiarity with GCP, IRB protocols, or clinical study documentation is a plus, but not required. We're glad to train the right person.
• Comfortable interacting directly with study participants in a professional, welcoming, and reassuring manner.
• Strong written communication skills for drafting clear, usable SOPs and study documentation.
• Organized and reliable with scheduling and logistics, including managing participant calendars and visit-day timing.

Physical Requirements

• Ability to sit or stand for extended periods during participant visits.
• Comfortable working in close physical proximity to study participants during fittings, measurements, and scans.

Contract Details

• Pay rate: $25-30/hour
• Schedule: Approximately 20 hours/week; specific days/hours will flex around scheduled participant visit days
• Duration: Approximately 4 months, with possible extension depending on study needs
• Classification: Part-Time, W-2
• Location: Hybrid, with on-site time required at Epia's Alameda, CA headquarters (400 Wind River Way, Suite 102, Alameda, CA 94501) for study visit days and required in-person collaboration.