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Be Well Clinical Studies

Full company profile

uuid003z9ib

Namestring
Be Well Clinical Studies
Legal namestring
Be Well Clinical Studies
Company typeenum
Private
Founded yearint
2018
Descriptiontext

Be Well Clinical Studies is a privately held clinical research site organization founded in 2018 and operated as part of the Be Well Health collaborative alliance alongside sister companies Be Well MD (in-home concierge medical practice for older adults) and Be Well Memory and Infusion (cognitive care and infusion therapies). The company operates two principal sites — the original Round Rock, Texas location (established 2018) and the Lincoln, Nebraska location (established 2020) — with an additional Omaha, Nebraska office, collectively providing Midwest and South geographic coverage. Its core service is conducting Phase II through IV clinical trials for pharmaceutical, biotechnology, and medical research sponsors, with therapeutic-area specialization in geriatric and senior-relevant conditions including Alzheimer's disease, vaccines, diabetes, heart failure, obesity, and gout.

The company's operating infrastructure includes exam rooms, on-site labs, dedicated pharmacy, refrigeration, freezers, refrigerated centrifuge, and locking drug storage, along with dedicated monitor space. It supports infusion therapies and vaccine studies, and operates under NIH Office of Science Policy oversight via its Institutional Biosafety Committee arrangement with Sabai IBC, enabling protocols that involve recombinant or synthetic nucleic acid molecules. The founder and director, Dr. Mark Carlson, is a fellowship-trained board-certified geriatrician, internist, and oncologist with over 30 years of healthcare experience and a track record as principal investigator on more than 60 clinical trials; the broader team carries 100+ years of combined research experience with a long history of collaboration. Each site maintains 2 Principal Investigators and 3 Sub-Investigators.

Revenue is generated under a professional-services model through per-subject fees, study management fees, and pass-through costs paid by trial sponsors. Named enterprise sponsors include GSK (for which the site contributed to RSV vaccine research leading to the first FDA-approved RSV vaccine), Pfizer, Bristol Myers Squibb, Amgen, and Life Molecular Imaging. Volunteer recruitment is driven through a dedicated website, a Refer-a-Friend program offering $100 per enrolled patient, virtual educational events hosted by Dr. Carlson, and outreach to a network of senior living communities (55+ apartments, independent living, and assisted living facilities). Volunteer compensation is per visit, loaded onto a card within 5 business days, with IRS Form 1099 issued for annual stipends exceeding $600.

Short descriptiontext

Be Well Clinical Studies is a private clinical research site organization operating in Nebraska and Texas, conducting Phase II–IV trials for pharma and biotech sponsors with a geriatric specialization and senior-living-community patient access network.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersLincoln, United States
HQ citystring
Lincoln
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical research site services, Phase II-IV clinical trials, vaccine clinical trials, Alzheimer's disease research, geriatric clinical research
Industry2 codes
1Clinical Trial Site Operations & Study Coordination
CodeHLAGACAEPrimaryYes
2Clinical Development (Phase I–III Trial Design & Execution)
CodeHLAIALAEPrimaryNo
NAICS code1 code
  • Scientific Research and Development Services5417
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Clinical Research Services
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Clinical Trial Conduct Services
TypeProfessional Services
Description

The company generates revenue by conducting clinical trials for pharmaceutical and biotechnology sponsors. They provide site facilities, recruit and manage study volunteers, collect data, and administer experimental treatments. Revenue is derived from per-subject fees, study management fees, and pass-through costs from sponsors.

bewellclinicalstudies.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Operations, Infrastructure, Marketing or Sales, Technology or R&D
Pricing details3 tiers
1Volunteer Stipend Compensation
ModelOtherBilling cadencePer visit
Notes

Volunteers are compensated for time and travel; Stipend payment loaded onto card within 5 business days from visit or call; Any amount greater than $600 in annual stipend reported to IRS with 1099 issued

bewellclinicalstudies.com
2Refer-a-Friend Bonus
ModelOtherBilling cadenceOne-time
Notes

$100 bonus for each newly enrolled patient referred

bewellclinicalstudies.com
3Pediatric RSV Study Compensation
ModelOtherBilling cadenceMulti-year contract
Notes

Enrolled participants may be compensated up to $3,750 for time and travel for several visits over 1-2 years

bewellclinicalstudies.com
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Be Well Clinical Studies operates as a clinical research site conducting Phase II-IV clinical trials for pharmaceutical and biotechnology sponsors. The company recruits study volunteers, administers experimental treatments including infusions and vaccines, collects clinical data, and provides on-site lab, pharmacy, and monitoring capabilities across therapeutic areas such as Alzheimer's disease, vaccines, diabetes, heart failure, obesity, and gout.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Be Well Clinical Studies is a clinical research organization operating as part of Be Well Health. The company provides a unified platform for clinical research trial services, connecting trial sponsors with volunteer participants. Their core offering consists of Clinical Research Trial Services (Phase II-IV trials), a Current Clinical Studies Platform listing active trials across multiple therapeutic areas (RSV, gout, obesity, Alzheimer's disease, diabetes, heart failure, vaccines, diabetic neuropathy), and Volunteer Recruitment Services for study participation. The company operates two research sites in the Midwest (Lincoln and Omaha, Nebraska) and South (Round Rock, Texas), serving trial sponsors with expertise in adult general medicine and geriatric care.

Product and service4 records
1Clinical Research Trial Services
CategoryClinical Research Services
2Volunteer Recruitment Services
CategoryClinical Research Services
3Current Clinical Studies Platform
CategoryClinical Research Services
4Trial Sponsorship Services
CategoryClinical Research Services
Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Be Well Clinical Studies is part of Be Well Health, a collaborative alliance dedicated to life-long health and wellness. This parent organization encompasses Be Well MD (in-home concierge medical practice), Be Well Clinical Studies (clinical trials for seniors), and Be Well Memory and Infusion (cognitive care and infusion therapies).

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Sister company; first to launch as an in-home concierge medical practice designed for older adults. Be Well MD provides medical care while Be Well Clinical Studies focuses on research trials for seniors.

Strategic tierSupportingTypeStrategic or Co-development Partner
Description

Sister company providing specialized cognitive care and infusion therapies, complementing the clinical research services of Be Well Clinical Studies.

Strategic tierSupportingTypeImplementation/ SI/ Consulting Partner
Description

Institutional Biosafety Committee services provider. Sabai IBC provides meeting minutes from convened IBC meetings conducted on behalf of the institution as required by NIH guidelines for research involving recombinant or synthetic nucleic acid molecules.

Strategic tierCoreTypeOthers
Description

Be Well Clinical Studies operates under NIH oversight as a registered site for Institutional Biosafety Committees (IBCs) conducting research involving recombinant or synthetic nucleic acid molecules.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Dr. Carlson was invited by Civitas Senior Living to share insights about influences of technology on senior health in their Civitas Speaker Series Chat.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global CRO with site network and patient recruitment capabilities. Comparable as a larger incumbent offering integrated clinical development and site services to pharma sponsors.

TypeDirect peer
Description

Tech-enabled clinical research site network providing access to patients through existing physician relationships. Comparable as a site-network competitor pursuing decentralized and community-based trial models.

3WCG
TypeBroad incumbent
Description

Provider of clinical research services including IRB, technology, and site support solutions. Comparable as a broader incumbent enabling and supporting clinical trial site operations across sponsors.

TypeBroad incumbent
Description

Largest global CRO with a substantial site management organization (IQVIA Site Solutions). Overlaps with Be Well as a broader incumbent offering end-to-end clinical development services including site operations.

TypeBroad incumbent
Description

Mid-size global CRO offering clinical trial management and site support. Comparable as a broader incumbent in the same clinical development services category.

TypeBroad incumbent
Description

Mid-to-large global CRO with dedicated clinical trial infrastructure and site coordination. Comparable as a broader incumbent competing for the same Phase II-IV sponsor business.

TypeBroad incumbent
Description

Global CRO formed via major consolidations (including PRA Health Sciences). Comparable as a broad incumbent with extensive site relationships and trial management capabilities.

TypeDirect peer
Description

Multi-therapeutic clinical research site network formed via roll-up of independent sites. Directly comparable business model and serves the same sponsor base for Phase II-IV studies.

TypeDirect peer
Description

Multi-site clinical research site network operating dedicated research facilities across the US. Strongly comparable as a directly competing independent site network performing Phase II-IV trials for pharmaceutical sponsors.

TypeDirect peer
Description

Privately held multi-site clinical research site organization. Comparable as a competing independent site network serving Phase II-IV trials across multiple therapeutic areas.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers5 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Be Well Clinical Studies

Clinical Research Servicesbewellclinicalstudies.com

Be Well Clinical Studies is a private clinical research site organization operating in Nebraska and Texas, conducting Phase II–IV trials for pharma and biotech sponsors with a geriatric specialization and senior-living-community patient access network.

What Be Well Clinical Studies does

Be Well Clinical Studies is a privately held clinical research site organization founded in 2018 and operated as part of the Be Well Health collaborative alliance alongside sister companies Be Well MD (in-home concierge medical practice for older adults) and Be Well Memory and Infusion (cognitive care and infusion therapies). The company operates two principal sites — the original Round Rock, Texas location (established 2018) and the Lincoln, Nebraska location (established 2020) — with an additional Omaha, Nebraska office, collectively providing Midwest and South geographic coverage. Its core service is conducting Phase II through IV clinical trials for pharmaceutical, biotechnology, and medical research sponsors, with therapeutic-area specialization in geriatric and senior-relevant conditions including Alzheimer's disease, vaccines, diabetes, heart failure, obesity, and gout.

The company's operating infrastructure includes exam rooms, on-site labs, dedicated pharmacy, refrigeration, freezers, refrigerated centrifuge, and locking drug storage, along with dedicated monitor space. It supports infusion therapies and vaccine studies, and operates under NIH Office of Science Policy oversight via its Institutional Biosafety Committee arrangement with Sabai IBC, enabling protocols that involve recombinant or synthetic nucleic acid molecules. The founder and director, Dr. Mark Carlson, is a fellowship-trained board-certified geriatrician, internist, and oncologist with over 30 years of healthcare experience and a track record as principal investigator on more than 60 clinical trials; the broader team carries 100+ years of combined research experience with a long history of collaboration. Each site maintains 2 Principal Investigators and 3 Sub-Investigators.

Revenue is generated under a professional-services model through per-subject fees, study management fees, and pass-through costs paid by trial sponsors. Named enterprise sponsors include GSK (for which the site contributed to RSV vaccine research leading to the first FDA-approved RSV vaccine), Pfizer, Bristol Myers Squibb, Amgen, and Life Molecular Imaging. Volunteer recruitment is driven through a dedicated website, a Refer-a-Friend program offering $100 per enrolled patient, virtual educational events hosted by Dr. Carlson, and outreach to a network of senior living communities (55+ apartments, independent living, and assisted living facilities). Volunteer compensation is per visit, loaded onto a card within 5 business days, with IRS Form 1099 issued for annual stipends exceeding $600.

Be Well Clinical Studies firmographics

Firmographics
Name
Be Well Clinical Studies
Legal name
Be Well Clinical Studies
Website
https://bewellclinicalstudies.com
Company type
Private
Founded year
2018
Operating status
Operating
Headcount range
11–50 employees
Short description
Be Well Clinical Studies is a private clinical research site organization operating in Nebraska and Texas, conducting Phase II–IV trials for pharma and biotech sponsors with a geriatric specialization and senior-living-community patient access network.
Ownership category
akta.pro rank

Be Well Clinical Studies industry classification

Industry
Product category
Clinical Research Services
NAICS
Scientific Research and Development Services (5417)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Clinical Trial Site Operations & Study Coordination (HLAGACAE)
akta.pro secondary industry
Clinical Development (Phase I–III Trial Design & Execution) (HLAIALAE)

Keywords

  • Clinical research site services
  • Phase II-IV clinical trials
  • Vaccine clinical trials
  • Alzheimer's disease research
  • Geriatric clinical research

Where Be Well Clinical Studies is headquartered

Location

Headquarters

HQ city
Lincoln
HQ country
United States
HQ region
North America

Offices3 records

Markets served

Be Well Clinical Studies business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Infrastructure, Marketing or Sales, Technology or R&D

Revenue model

  1. Clinical Trial Conduct Services: The company generates revenue by conducting clinical trials for pharmaceutical and biotechnology sponsors. They provide site facilities, recruit and manage study volunteers, collect data, and administer experimental treatments. Revenue is derived from per-subject fees, study management fees, and pass-through costs from sponsors.

Pricing tiers

ModelBillingPrice
OtherPer visitVolunteer Stipend Compensation
OtherOne-timeRefer-a-Friend Bonus
OtherMulti-year contractPediatric RSV Study Compensation

Go-to-market motion2 records

Distribution channels1 record

Marketing channels5 records

Be Well Clinical Studies product offering

Product offering

Core offering

Be Well Clinical Studies operates as a clinical research site conducting Phase II-IV clinical trials for pharmaceutical and biotechnology sponsors. The company recruits study volunteers, administers experimental treatments including infusions and vaccines, collects clinical data, and provides on-site lab, pharmacy, and monitoring capabilities across therapeutic areas such as Alzheimer's disease, vaccines, diabetes, heart failure, obesity, and gout.

Product overview

Be Well Clinical Studies is a clinical research organization operating as part of Be Well Health. The company provides a unified platform for clinical research trial services, connecting trial sponsors with volunteer participants. Their core offering consists of Clinical Research Trial Services (Phase II-IV trials), a Current Clinical Studies Platform listing active trials across multiple therapeutic areas (RSV, gout, obesity, Alzheimer's disease, diabetes, heart failure, vaccines, diabetic neuropathy), and Volunteer Recruitment Services for study participation. The company operates two research sites in the Midwest (Lincoln and Omaha, Nebraska) and South (Round Rock, Texas), serving trial sponsors with expertise in adult general medicine and geriatric care.

Differentiator

Problem solved

Functional benefit

Products and services

  • Clinical Research Trial Services
  • Volunteer Recruitment Services
  • Current Clinical Studies Platform
  • Trial Sponsorship Services

Companies that use Be Well Clinical Studies

Customer profile

Named customers5 records

Segments3 records

Ideal customer profiles2 records

Be Well Clinical Studies technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Be Well Clinical Studies partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered core, supporting and minor.

  • Be Well HealthcoreStrategic or Co-development PartnerBe Well Clinical Studies is part of Be Well Health, a collaborative alliance dedicated to life-long health and wellness. This parent organization encompasses Be Well MD (in-home concierge medical practice), Be Well Clinical Studies (clinical trials for seniors), and Be Well Memory and Infusion (cognitive care and infusion therapies).
  • Be Well MDcoreStrategic or Co-development PartnerSister company; first to launch as an in-home concierge medical practice designed for older adults. Be Well MD provides medical care while Be Well Clinical Studies focuses on research trials for seniors.
  • Be Well Memory and InfusionsupportingStrategic or Co-development PartnerSister company providing specialized cognitive care and infusion therapies, complementing the clinical research services of Be Well Clinical Studies.
  • Sabai IBCsupportingImplementation/ SI/ Consulting PartnerInstitutional Biosafety Committee services provider. Sabai IBC provides meeting minutes from convened IBC meetings conducted on behalf of the institution as required by NIH guidelines for research involving recombinant or synthetic nucleic acid molecules.
  • NIH Office of Science PolicycoreOthersBe Well Clinical Studies operates under NIH oversight as a registered site for Institutional Biosafety Committees (IBCs) conducting research involving recombinant or synthetic nucleic acid molecules.
  • Civitas Senior LivingminorGTM or Marketing PartnerDr. Carlson was invited by Civitas Senior Living to share insights about influences of technology on senior health in their Civitas Speaker Series Chat.

Scale indicators6 records

Recent moves6 records

Expansion highlights5 records

Be Well Clinical Studies competitors and assessment

Company assessment

Broad incumbents

  • Syneos Health: Global CRO with site network and patient recruitment capabilities. Comparable as a larger incumbent offering integrated clinical development and site services to pharma sponsors.
  • WCG: Provider of clinical research services including IRB, technology, and site support solutions. Comparable as a broader incumbent enabling and supporting clinical trial site operations across sponsors.
  • IQVIA: Largest global CRO with a substantial site management organization (IQVIA Site Solutions). Overlaps with Be Well as a broader incumbent offering end-to-end clinical development services including site operations.
  • Clinipace Worldwide: Mid-size global CRO offering clinical trial management and site support. Comparable as a broader incumbent in the same clinical development services category.
  • Medpace: Mid-to-large global CRO with dedicated clinical trial infrastructure and site coordination. Comparable as a broader incumbent competing for the same Phase II-IV sponsor business.
  • ICON plc: Global CRO formed via major consolidations (including PRA Health Sciences). Comparable as a broad incumbent with extensive site relationships and trial management capabilities.

Direct peers

  • Elligo Health Research: Tech-enabled clinical research site network providing access to patients through existing physician relationships. Comparable as a site-network competitor pursuing decentralized and community-based trial models.
  • Flourish Research: Multi-therapeutic clinical research site network formed via roll-up of independent sites. Directly comparable business model and serves the same sponsor base for Phase II-IV studies.
  • Velocity Clinical Research: Multi-site clinical research site network operating dedicated research facilities across the US. Strongly comparable as a directly competing independent site network performing Phase II-IV trials for pharmaceutical sponsors.
  • Accel Clinical Research: Privately held multi-site clinical research site organization. Comparable as a competing independent site network serving Phase II-IV trials across multiple therapeutic areas.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Be Well Clinical Studies social profiles

Digital presence

Be Well Clinical Studies financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Be Well Clinical Studies leadership team

Management profile

Number of profiles

Profiles2 records

Be Well Clinical Studies funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Be Well Clinical Studies M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Be Well Clinical Studies

What does Be Well Clinical Studies do?

Be Well Clinical Studies operates as a clinical research site conducting Phase II-IV clinical trials for pharmaceutical and biotechnology sponsors. The company recruits study volunteers, administers experimental treatments including infusions and vaccines, collects clinical data, and provides on-site lab, pharmacy, and monitoring capabilities across therapeutic areas such as Alzheimer's disease, vaccines, diabetes, heart failure, obesity, and gout.

Is Be Well Clinical Studies a public or private company?

Be Well Clinical Studies is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was Be Well Clinical Studies founded?

Be Well Clinical Studies was founded in 2018. It employs 11 to 50 people.

Where is Be Well Clinical Studies based?

Be Well Clinical Studies is headquartered in Lincoln, United States, in the North America region.

How does Be Well Clinical Studies make money?

One revenue line is on record: clinical Trial Conduct Services.

Who are Be Well Clinical Studies's main competitors?

Broad incumbents on record are Syneos Health, WCG, IQVIA, Clinipace Worldwide, Medpace and ICON plc. Direct peers are Elligo Health Research, Flourish Research, Velocity Clinical Research and Accel Clinical Research.

Does Be Well Clinical Studies have an API?

No public API is recorded for Be Well Clinical Studies.

What industry is Be Well Clinical Studies in?

Be Well Clinical Studies's product category is Clinical Research Services. Its primary akta.pro industry code is HLAGACAE, Clinical Trial Site Operations & Study Coordination, with a secondary code of HLAIALAE, Clinical Development (Phase I–III Trial Design & Execution). Its NAICS code is 5417 and its SIC code is 8731.

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