Three reasons physicians who do research partner with NeoSci

Physician reviewing clinical research data

More research dollars in your pocket.

Most CROs take 40–50% of your study budget and never tell you. NeoSci shows you the full budget and puts 55% directly in your hands.

We find studies that fit your practice.

Navigating pharma to land a new study is a full-time job. NeoSci identifies the opportunities, builds the relationships, and delivers contracted studies ready to run.

We handle patient recruitment for every study.

NeoSci runs targeted campaigns, screens candidates for eligibility, and coordinates visit scheduling — so your site stays on timeline and your pipeline stays full.

Schedule a Conversation
Medical team collaboration

A Clear Division of Responsibilities

NeoSci Provides

Study opportunities & business development
Budget & contract negotiation with sponsors
Complete site setup & regulatory
Clinical Trial Management System (CTMS)
Staff training — GCP, protocols, compliance
Ongoing quality assurance & monitoring
Patient recruitment support*

Physician Partner Provides

Principal Investigator (PI) role
Clinical coordinator from your staff
Sub-investigators & other staff as required
Perform procedures per protocol
Patient recruitment from your base
Patient data collection

Site Requirements

What Your Practice Needs

Most private practices already have the essentials.

Medical office space
A

Patient Exam Space

Dedicated or shared exam room for research patient visits — your existing rooms work. Schedule around normal patient flow.

B

Coordinator Workspace

Desk with PC and reliable internet access for your study coordinator. Used for data entry, eCRF, and electronic source documents.

C

Conference / Monitor Room

Room for sponsor monitor visits, site initiation visits, and training sessions. Can double as a break room or office.

D

Secure Drug Storage

Lockable room with lockable cabinet for investigational product. Dedicated secure refrigerator, freezer, and ambient storage with temperature monitoring.

E

Lab / Sample Processing

Centrifuge and basic lab supplies for specimen processing. Dedicated secure refrigerator and freezer for sample storage before shipment to central lab.

F

Additional Requirements

Reliable phone/fax line, secure filing for regulatory binders, adequate parking for research patients, and after-hours patient contact process.

How It Works

Your Path to Clinical Research Revenue

Physicians collaborating
01NeoSci

Contracting

Execute agreements and regulatory documents.

02NeoSci

Site Setup

Prepare your office with required equipment and technology infrastructure.

03NeoSci

Staff Training

Your team trained on protocols, GCP, documentation, and compliance.

04NeoSci

Study Matched

We bring pharma-sponsored studies aligned to your specialty.

05Partner

Enroll Patients

Recruit from your existing patient base. We support recruitment.

06Partner

Conduct & Earn

Execute the protocol, collect data, receive payment.

Illustrative Example

What a Study Could Mean for You

Sample Asthma / Allergy Biologic Study

Phase III — Novel Therapy

Per-patient revenue$10,000 – $20,000
Target enrollment15 patients
Total study revenue$150,000 – $300,000
Your share (55%)$82,500 – $165,000
Study duration~24–52 weeks
$82,500 –
$165,000
Your estimated revenue from a single study
Multiple concurrent studies = multiply this number

Illustrative only. Actual results vary by study design, enrollment, and contract terms.

Frequently Asked Questions

What Physicians Want to Know

Q

Will clinical research disrupt my patient care?

No. Studies are scheduled around your practice flow. Research visits use existing exam rooms during available time slots. Your primary care operations remain the priority.

Q

How long before I start earning revenue?

Site setup typically takes 4–8 weeks. Revenue begins with your first enrolled patient. NeoSci pays within 15–30 days of receiving sponsor payment.

Q

How much of my time is required as PI?

Typically 15–30 minutes per patient visit for oversight, plus protocol-specific assessments. NeoSci and your trained coordinator handle the administrative burden.

Q

What happens if a study is cancelled mid-trial?

Sponsors pay for all work completed through the cancellation date. You are compensated for every patient visit and procedure already performed.

Q

What if a study isn't a good fit for my practice?

You have full approval rights on every study. NeoSci matches opportunities to your specialty, patient demographics, and capacity. You never have to accept a study.

Q

Do I need prior research experience?

No. NeoSci provides comprehensive GCP training, protocol-specific training, and ongoing mentorship. Many successful PIs started with zero research background.

About NeoSci

40+ Years of Clinical Research Experience

The NeoSci team has deep experience across every facet of clinical research — from Pharma study acquisition and contract negotiation to study management in a physician's office to patient recruitment and retention.

Therapeutic Areas

PsychiatryAsthma & AllergyPainVaccinesGastrointestinalDermatologyAnd More
Physician in clinical setting
40+Years Combined Experience
55%Revenue to Physician Partners
100%Budget Transparency

Get Started

Ready to Put More Research Dollars in Your Pocket?

Let's start with a confidential conversation about how clinical research can become a profitable part of your practice — with zero upfront cost.

contact@neosciclinicalresearch.com
+1 (435) 709-6266
NeoSci on LinkedIn
NeoSci Clinical Research
6543 N. Landmark Drive, Suite 1177
Park City, UT 84098