Connect your lab to the clinic.
We build and run the pipeline that brings human samples from clinical settings to research laboratories, with the clinical metadata that makes them useful.
Project managers and clinical research coordinators who launch, coordinate, and manage your research: biospecimen pipelines, clinical studies and trials, and complex scientific programs. We join at the point the work needs us, for as much effort as it needs.
We build the pipeline from clinic to bench: clinical collaborators, protocol and regulatory approvals, consent, collection, processing, and handoff to your lab or UCSF CoLabs, with clinical metadata that travels with every sample.
Each is a distinct capability, and none is a career stage of another. Most engagements draw on more than one: the same coordinators often deliver both clinical and biospecimen work, and project managers support basic, clinical, and translational science alike.
We build and run the pipeline that brings human samples from clinical settings to research laboratories, with the clinical metadata that makes them useful.
Coordinators who take a protocol from feasibility through activation, enrollment, and close-out, for investigator-initiated and industry-sponsored studies alike.
Project and program managers who run the operational side of multi-investigator and multi-institutional science, in basic, clinical, and translational work.
The same operating rhythm applies to a clinical trial and a multi-institutional program. What changes is the mix of people: coordinators for human-subjects work, project managers for the program around it, data managers alongside both.
We learn the scientific objectives and what delivering them will take: feasibility, clinical partners, the regulatory path, staffing, infrastructure, and budget. You leave with a scoped plan and a realistic read on timeline.
Protocols, IRB and regulatory submissions, contracts and activation, workflows and SOPs, databases, and the coordination structure the work will run on, whether that is a study team or a consortium's governance.
Day-to-day coordination: visits, samples, milestones, budgets, reporting, and quality control. We resolve operational problems as they arise, keep investigators informed, and hand over a dataset that is ready when the science is.
We learn the scientific objectives and what delivering them will take: feasibility, clinical partners, the regulatory path, staffing, infrastructure, and budget. You leave with a scoped plan and a realistic read on timeline.
Protocols, IRB and regulatory submissions, contracts and activation, workflows and SOPs, databases, and the coordination structure the work will run on, whether that is a study team or a consortium's governance.
Day-to-day coordination: visits, samples, milestones, budgets, reporting, and quality control. We resolve operational problems as they arise, keep investigators informed, and hand over a dataset that is ready when the science is.
Below, each service with a few of the projects and programs our team runs today. The full list is on Programs & Projects.
active programs and projects in 2025, up from 10 in 2023, across 12+ departments, divisions, and programs.
Pipelines that bring tissue, blood, and other samples from UCSF clinics to research labs and CoLabs.
Coordinators on clinical trials and human-subjects studies, from startup and consent through study visits.
Managers running consortia, multi-project programs, and the operations of clinical research units.
Many projects draw on more than one service; coordinators often deliver both clinical and biospecimen work, so category counts overlap.
Biospecimen pipeline awards“OCR engages with and supports the UCSF community. The ‘collaboration’ in its name reflects exactly what it does: connecting people and building interdisciplinary partnerships. I’ve come to see OCR as a source of innovation.”
“OCR exemplifies what makes UCSF great. Grassroots organizations like OCR are essential to building a stronger, more connected research community.”
Investigators and institutional partners work with our staff in whatever form fits the project. In every form, our staff join as part of the research team: they learn the science, stay with the project, and leave behind workflows the group can keep running.
A coordinator or manager at the fraction of effort a single project needs, rather than a full-time position.
Staff supported by an award or an institutional partnership, embedded with your team for the life of the work.
Coordinators who work across several related studies, so smaller projects get experienced coverage.
Senior coordinators who bring structure, supervision, and standard workflows to a clinical research unit you already have.
Data management, research development, and community management when the project calls for them.
Six people who work across studies and programs, so each project gets experienced support at the effort it needs.







Runs study startup, milestones, and operations across consortium projects. Keeps the work moving without losing the science.

Senior CRC on autoimmune and inflammatory cohorts. IRB, consent, and chart abstraction.

Supports enrollment, consent, and day-to-day study operations across OCR clinical portfolios.

Coordinates patient enrollment and biospecimen workflows across UCSF clinics.

Patient-facing coordination and study operations for human-subjects research.

Coordinates participant visits, consent, and day-to-day study operations for OCR clinical portfolios.
Partners hold dedicated capacity on our team; other UCSF investigators are supported as bandwidth allows.
You can bring us in at any point: early planning, study startup, an active study, or a program that is expanding or restructuring. The earlier the conversation, the more options we have.
Choose a stage and we'll tell you what is useful to include in a first email.