Clinical Operations Lead
Confirmed on the employer's own hiring board on Oct 27, 2026. First seen by Alion on Sep 3, 2026. Convergent Research scores A on the Alion truth index.
About Arbor Neuroscience
(formerly Forest Neurotech)
Arbor is a nonprofit research organization working on one of the hardest open problems in clinical neuroscience: how to change brain circuits by design.
Millions of people with depression, chronic pain, and other brain disorders have no treatment that works. Modulating activity in the brain circuits underlying their symptoms - with electrical stimulation, focused ultrasound, or magnetic stimulation - can work spectacularly well. But it doesn't work reliably, and we can't predict who it will help.
That's what Arbor aims to fix. The starting point is a new class of experiment: intervene, measure how the circuit responds, track the symptom, and repeat in the same individual over months. We’re building the necessary experimental platform. It currently includes the Forest 1 ultrasound system, which works like a wearable functional MRI, but with higher resolution. The system images activity across large brain volumes, including deep brain structures, and will soon stimulate as well. We are also adding electrode-based interfaces in animal studies. From these data, we'll build models to make neuromodulation predictable.
Arbor is a Focused Research Organization within the Convergent Research family, and the new name for Forest Neurotech. We're a mission-focused nonprofit, doing multidisciplinary translational work that doesn't fit in a lab or on a company roadmap. We have the funding to run the first phase, and we're a small team - the people we hire now will shape what Arbor becomes.
The Role
This is the person who makes sure we can actually run studies with human participants.
Arbor's human studies use functional ultrasound imaging, and soon focused ultrasound neuromodulation. Participants are people with a sonolucent cranial implant, usually placed after surgery for traumatic brain injury, stroke, or a tumor. The studies are longitudinal: the same participant returns over months, first in the lab or clinic and eventually at home. We work in partnership with hospitals and academic centers, here and in the UK.
The program needs to grow, and much of the infrastructure for that doesn't exist yet.
Part of the job is conventional clinical operations: IRB submissions and amendments, protocol preparation, site readiness, participant scheduling and support, safety monitoring, documentation, and training systems. You'd own all of it. We're small, so for now that means doing the work as much as overseeing it.
The second part is harder to specify and a bigger challenge. Our program will depend on the quality and scale of our relationships with clinicians and hospital departments. Building and maintaining those partnerships requires a real understanding of where our interests align. This would be yours to own.
You'd also help grow our studies beyond the clinic. At-home longitudinal neuromodulation is where this program is headed, and we don’t yet know what that requires. Some of the answers are technical, and some will come from spending time with participants and seeing what their lives are like at home.
What You’ll Do
Partner with scientific leadership on clinical strategy: which sites and partnerships and where our incentives align
Develop and own a recruitment program from a small and geographically scattered participant pool
Qualify and onboard clinical partners
Help design what at-home studies will require, from participant experience through logistics and safety
Lead start-up for internal and external studies
Own our IRB submissions and ongoing interactions
Manage participant scheduling, visits, follow-up, payments, and travel
Coordinate device deployment, equipment readiness, and study-specific technical support; you don't need to run experiments, but you should be able to troubleshoot them
Establish and maintain TMF, document control, clinical SOPs, and the personnel training program
Own adverse event tracking and reporting
Build the clinical program:
Run the studies:
Where you start will depend on your strengths and on what the program needs most. This won't stay one person's job as Arbor grows.
Who We’re Looking For
Substantial experience in human clinical research operations
Enough scientific training to engage substantively with clinicians and researchers and to step in and help run a study when we need it. Advanced training, ideally a PhD in a relevant field, is the most common route, but not the only one
The written and spoken communication skills to explain the research to participants and collaborators and to produce final drafts of key documents
The organizational and interpersonal skills to keep everyone moving in the same direction, often with no established process to follow
The ambition to build clinical infrastructure, not just run it
Directness without friction - you say what you think, ask when you don't know, and aren't looking to compete with your colleagues
The successful candidate will have:
Nice to have: background in neuroscience, neuroimaging, neuromodulation; work with hospitals, academic medical centers, or external clinical research partners; early-stage medical device or biotech experience; familiarity with ICH-GCP, ISO 14155, and FDA medical device requirements; experience with QMS, CTMS, or eTMF systems; AE/SAE reporting, monitoring, CAPAs, and audit readiness.