For Sites

Built for sites that run trials.

Tools and templates for clinical trial sites — coordinator and investigator checklists, startup documents, and a site-level budget estimator. Free to start.

Today — free

What you can use right now

Coming with platform launch

What we are building for sites

Use cases

How sites actually use AVD today

Resources for Sites

Templates you can use today

GCP-aligned SOPs and checklists designed for site coordinators, investigators, and study staff.

FAQ

Questions from site coordinators & investigators

Do I need to pay for anything to get started?+

No. The Resource Library and your first Budget Calculator report are free. Paid options start at $9 for a single SOP or report if you want more.

Are the SOPs ready to use at my site as-is?+

No, and that's intentional. They're starting frameworks with placeholders (sponsor name, effective date, document owner, local regulatory environment) that need customization and review by a qualified QA professional before use at your site.

What's in the Site Startup Bundle?+

12 templates for $79: Site Qualification and Site Initiation Visit checklists, Delegation of Authority log, staff training log, regulatory binder checklist, and essential documents checklist.

Is there a live site dashboard or management platform?+

Not yet. The site dashboard, procedure tracker, SC timeline tracker, and role-based accounts above are on our roadmap. Live today: the free Library, Budget Calculator, and SOP marketplace, all with email OTP sign-in.

Can we get direct support for site activation or monitoring?+

Yes. We take on site activation, SOP authoring, budget modelling, and feasibility support as scoped project work, separate from the self-serve templates and calculator. See Site Management Services above.

Site Management Services

Full-service SMO support — without the overhead

Templates solve the blank page. Sometimes you need someone to actually do the work. AVD Clinical takes on site management as direct project work — senior-led, scoped to what you need, and priced so a single site can afford it.

Why sites choose us

Big SMOs are built for portfolios of sites and priced accordingly. We're built for the site that needs a specific problem solved — startup that's slipping, a budget that doesn't add up, an SOP set that won't survive a monitoring visit. You work directly with the people doing the work. No account managers, no minimum portfolio, no 40-page MSA before anyone starts.

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Site startup & activation

Regulatory binder build, essential document collection, delegation logs, training records, SIV preparation, and activation readiness review — so your green light isn't held up by paperwork.

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SOP & document authoring

Your SOP set, written for how your site actually works — not a generic pack. Version-controlled, review-dated, and built to hold up when a monitor or auditor asks.

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Budget development & negotiation support

Per-patient costing, pass-through separation, screen-failure modelling, and a defensible position for your sponsor conversation. Every assumption is written down, so you can argue it line by line.

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Feasibility & study capture

A reusable site capability profile plus support answering feasibility questionnaires properly — realistic numbers, sourced, and framed to win the studies you can actually deliver.

How we work: scoped project work with a written deliverable and a fixed quote — not an open-ended retainer. We'll tell you honestly if a template you can buy for $9 solves your problem instead. Every document we produce is a starting framework your QA function reviews and approves before operational use; AVD Clinical does not certify regulatory compliance.
Talk to us about your site →

Tell us the problem in a sentence. We'll tell you if we're the right fit — and if we're not, we'll say so.

Partner with us

Three ways to work with AVD Clinical

Whether you need people, need to get research-ready, or want a steady pipeline of studies — there's a route in. Start wherever you are.

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1 · Staffing & resourcing

Now onboarding — East Coast first. Need a coordinator for a startup crunch, cover for leave, or a monitor for a few visits? We place experienced clinical research staff with your site, short-term or ongoing, so a resourcing gap doesn't stall a study.

Request staffing support →

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2 · Training & onboarding

Available nationwide. New to research, or restarting after a gap? We get your site study-ready: SOP set, regulatory binder, delegation and training structure, and hands-on onboarding for your team — delivered remotely, so where you are doesn't matter.

Get your site study-ready →

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3 · Join the Site Network

Open to sites anywhere. Work with us exclusively and we bring the studies to you. Your capability profile goes in front of sponsors and CROs, and you get full operational support running them — feasibility, startup, budgets, and documentation handled alongside your team.

Apply to join the network →

Why network sites win more studies

Sponsors don't want to negotiate with six sites separately. Across our network we offer them one point of contact, one IRB submission, and one budget — so a multi-site study becomes one conversation instead of six. That's a genuine reason for a sponsor to choose our sites, and it means studies reach you that you'd never have been shortlisted for alone.

Straight about stage: on-site staffing placement is East Coast first and expanding from there. Training, onboarding and network membership are available to sites anywhere — both are delivered remotely. Network membership is selective: we take sites we believe we can genuinely keep busy, and we'd rather say no than sign you up and deliver nothing. Every arrangement is a written agreement; nothing here changes your regulatory obligations as a site.
What's next

We're expanding — tell us where you need us

Our staffing and site network start on the East Coast, and we're opening new regions based on where demand actually is. If that isn't your area yet, tell us — the regions we hear about most are the ones we open next.

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Not in your region yet?

On-site staffing is East Coast first — but training, onboarding and Site Network membership are open to you today, wherever you are. Tell us your region and we'll prioritise it for staffing as we expand.

Tell us your region →

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Need something we haven't listed?

Our services grew out of what people asked us for. If you need something adjacent to what's here, ask — we'll either take it on, or tell you straight that it isn't us and point you somewhere better.

Ask us about a service →

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Stay in the loop

New regions, new services, and new free templates as they launch. One short email a month, no spam, unsubscribe any time.

Keep me posted →

Get started

Use the free Library and Calculator today. Sign up below to be the first to know when the site platform launches.

Work with us

Connect with AVD Clinical

Interested in a project partnership? Whether you need partial support or full end-to-end clinical trial services, we'd love to hear from you.

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Call us

+1 929-502-4973
Mon–Fri, 9am–6pm ET

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Email us

[email protected]
Response within 1 business day

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Project inquiry

Site activation, monitoring support, SOP authoring, budget modeling, or full study coordination — tell us what you need →