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Welcome To CRA
Experienced sites proven results

"I have worked with CRA for 20 years! We've been through many data-locks and FDA audits together. Because of their professionalism, attitude toward research, excellent regulatory management, and flexibility, I wish ALL of my studies took place at a CRA office. What a delight they are to work with!"

- Lynda C., Sr. Clinical Site Monitor, Bristol-Myers Squibb

"Site personnel are pleasant and responsive to work with; their efforts in recruitment have been terrific and greatly appreciated. Nice site to work with!"

- Midge F., RN, CCRA, Biogen Idec

"Each and every study coordinator that I've worked with at CRA shows experience, critical thinking, and the utmost courtesy. It's reassuring to know that I can expect the same quality and dedication from each site affiliated with CRA Studies!"

- April O., Regional Clinical Research Associate, Takeda

Operational Model

Therapeutic Area of Experience

Investigator Experience

Locations

Pharma Sponsor Partners

Industry Professionals

Why use Clinical Research Advantage?

Clinical Research Advantage, Inc. has provided experienced research sites to the Pharmaceutical and medical device industry for over 18 years, making us one of the most senior Trial Management Organizations (TMO) in the nation.

Our key to success is the relationships we've established by integrating ourselves into existing medical practices.

Our primary source for patient recruitment comes from the existing patients that are seen in our individual clinics.

Clinical Research Advantage's expertise provides our sponsors with consistent subject enrollment, evaluable patients, complete and accurate data and a high retention rate.

Services Offered

Clinical Research Advantage offers professional and experienced staff including:

Family Practice and Internal Medicine Physicians
Neurologists
Dermatologists
ENTs
Rheumatologists
Pulmonologists
Physician Assistants
Registered Nurses
Clinical Research Coordinators
Research Assistants
Support Personnel

Clinical Research Advantage offers a variety of valuable services to our sponsoring companies such as:

Study coordination services for Phase II-IV clinical trials
Prompt preparation of site regulatory documents including IRB submissions
Rapid budget and contract negotiations
Start-up and source development department
Strict protocol adherence and regulatory compliance
Dedicated regulatory and quality assurance staff
Full-time trained staff dedicated solely to research
Rapid enrollment of qualified study participants
Ongoing study site quality assurance
Complete confidentiality
Round the clock medical research coverage
Paper or electronic CRF capabilities
Electronic diary experience

Therapeutic Areas

AECB
Allergic Rhinitis
Alzheimer's
ALS
Asthma
Birth Control
Diabetes
ED
Epilepsy
GERD
Hyperlipidemia
Hypertension
IBS
Insomnia
Lupus
Migraines
MS

OA
Osteoporosis
Obesity
Pain Management
Parkinson's
PHN
RLS
Sinusitis
Smoking Cessation
Vaccines
- Influenza
- Hepatitis
- HPV
- HSV
- Pneumonia
- More...

Facility Description

Each of our research facilities are approximately 10,000 square-feet with 10-30 medical professionals and state-of-the-art equipment.

Dedicated research exam rooms
On-site laboratory facility
IATA certified staff
Minus 20 and minus 70 Freezer with access to dry ice
PFT machines
Double locked, temperature controlled drug storage
ECG machines
X-ray facilities
DEXA scanning capabilities
Monitor rooms with copier, phone, and high speed Internet access
Holter monitoring capabilities
Female examination capabilities