DSCS works directly with independent clinical research sites — handling study acquisition, budget negotiation, regulatory startup, and ongoing operations support. Your site stays in control. We do the heavy lifting.
Get Started →One flat monthly fee. No upsells. No hourly billing. DSCS covers the full scope of site operations support — from first feasibility to patient visit.
DSCS services are designed specifically for sites that don't have a 50-person ops team. You have a consultant in your corner — not a system to learn.
DSCS reaches out to sponsors on your behalf, identifies studies that match your site profile, and guides you through the feasibility process to maximize selection.
Using a proven strategy developed across hundreds of studies, DSCS negotiates budgets and contracts that protect your site's interests. You remain the payee — not a study broker.
From IRB submission guidance to regulatory packet completion, DSCS walks your team through every document needed to get a study open and running.
GCP certification, NIH training, IATA dangerous goods — DSCS provides links and guidance so your team meets sponsor requirements before the SSV.
Paper source documents created for any study your site acquires through DSCS. Included at no additional cost — no per-study fees.
Unlimited phone access to your own private DSCS consultant. Questions don't wait for a ticket queue — you pick up the phone and get answers.
Clinical trials create a direct path to new patient referrals. DSCS's model is designed to help independent sites turn research participation into practice growth.
Starting from scratch? DSCS provides initial Standard Operating Procedure templates tailored to independent research site requirements.
DSCS follows a structured, repeatable process that gets sites from zero to study-ready — and keeps them there.
Your dedicated consultant kicks off with an onboarding call. You receive GCP and IATA training links, guidance on office layout and equipment requirements, and initial SOP assistance to get your site set up correctly from day one.
DSCS collects your Principal Investigator information, CV, address, patient demographics, and therapeutic area focus. This builds your site profile — used to target the right sponsors and studies for your patient population.
DSCS submits continuous study applications on your behalf and delivers weekly inquiry reports — so you always know which sponsors have reviewed your site and where you stand in the selection process.
When a sponsor wants to visit your site, DSCS prepares you. Pre-SSV guidance covers everything sponsors evaluate — documentation, staff credentials, facility readiness, and protocol-specific questions.
DSCS negotiates directly with sponsors using a proven strategy built on years of industry experience. Critically: your site remains the payee. You're not handing revenue to a broker — you own the contract and the budget.
DSCS guides your team through completing the regulatory packet — IRB submissions, delegation of authority logs, financial disclosures, and all sponsor-required startup documents — so you don't miss anything that delays activation.
At no additional cost, DSCS creates paper source documents for every study your site acquires. Custom to the protocol, ready for monitoring visits, included in your flat monthly fee.
The process repeats continuously. DSCS maintains active outreach to sponsors on your behalf, submits new feasibilities as studies come available, and keeps your pipeline growing — month after month.
$1,500/month. No contract. Dedicated consultant. Everything your site needs to acquire, activate, and run clinical trials — handled by people who've done it for 25+ years.
Get Started with DSCS →