Why Work with NWCRC? - Northwest Clinical Research Center

History and Experience

With over 30 years of experience, Northwest Clinical Research Center has conducted numerous studies across various indications, with more than 750 clinical trials, contributing to the approval of over 40 drugs. We are dedicated to providing the highest quality medical research services and interim care (before and after studies) to our patients. We are proud to have provided services such as clinical evaluations, diagnostic tests, care management, and educational guidance to the community since 1995 by partnering with the pharmaceutical industry on research endeavors.

Patient safety is our top priority and we ensure all patients feel welcome regardless of entry into a clinical trial. Experience, specialized expertise, and appreciation for our patients underscore every service we provide.

Current Capabilities:

Over 50 ongoing clinical studies
Expertise in multiple therapeutic areas, including neurological, psychiatric, pediatric, metabolic, and women’s health.
State-of-the-art facilities are equipped with comprehensive clinical research.

NWCRC-Privacy-Notice-2021.pdf

Dedicated Research Staff

NWCRC employs a highly experienced and specialized research team to ensure high-quality study execution:

Arif Khan, MD NW Clinical Research Center

7 Board-Certified (Principal Investigators) Physicians, including Internal medicine, Family, OBGYN, Psychiatry and Neurology specialties.
Our PIs collaborate closely with and consult with sponsors on study design and protocol development.
5 Licensed Medical Sub-Investigators
3 Dedicated Raters (experienced in psychiatric, neurological, and cognitive assessments) Additional raters as needed
2 Dedicated Lab Associates (certified phlebotomists)
10+ Study Coordinators (experienced in multi-therapeutic trials)
7 Regulatory Coordinators (ensuring IRB and compliance readiness)
6 Dedicated Recruitment Coordinators (specializing in patient outreach and engagement)
On-Site Unblinded Staff (for investigational product (IP) management)
On-Site locked secure IP storage room, include controlled substance, with continuous temperature monitoring, and aseptic laminated preparation hood.

Our staff’s combined expertise allows us to efficiently manage clinical trials while ensuring compliance, patient safety, and data integrity.

Our state-of-the-art facility, highly experienced investigators, and dedicated study teams ensure efficient study execution, protocol adherence, and superior patient care. We consistently hit or exceed enrollment targets, making us a reliable and high-performing site for sponsors and CROs.

At NWCRC we diligently follow the Good Clinical Practice, FDA recommendations, study protocol and IP manual instructions to accurately prepare IP, ensuring reliability throughout the trial. Our staff meticulously reviews the investigator’s brochure and relevant documentation to gain a deep understanding of the IP properties, handling requirements, and administration guidelines. When required, our staff can compound IP according to study specifications, ensuring precise formulation and dosing. Our team employs proper aseptic techniques to minimize contamination risks and maintain the integrity of the IP. We maintain detailed records of IP preparation, including lot numbers, expiration dates, and any deviations or issues encountered during the process.

Why NWCRC?

Proven Track Record – With over 30 years of experience and contributions to the approval of over 40 drugs, NWCRC is a trusted and experienced research site.
High Enrollment Performance – We consistently meet or exceed enrollment targets, ensuring studies stay on track and meet recruitment goals.
Patient Access – Established recruitment channels through local partnerships, outreach programs, and social media presence.
Comprehensive Research Capabilities – Our team is highly experienced in managing infusions, injections, device trials, immunizations, and various forms of self-administered medications. We excel in IP preparation, including aseptic technique.

State-of-the-Art Facility – Our 16,000 sq. ft. research center includes 25+ patient rooms, an infusion suite, an on-site lab, and dedicated IP storage and management, with 8 monitors capacity per day.
Child, Family, and Pet-Friendly capacity, with accommodation for patients with disabilities and special transportation needs.
Streamlined Regulatory & Contracting Process – We begin regulatory submissions immediately after budget and contract finalization, typically within 3–5 business days. NWCRC works with all central IRBs, avoiding local IRB delays. In 2024, we had two FDA audits with no findings, reflecting our commitment to compliance and data integrity.

Serving You Locally

We are located in the heart of Bellevue, Washington. We are easily accessible from Seattle and the Greater Puget Sound area, and conveniently located near the 520 freeway with a public bus stop in front of our building and plenty of free parking.

NWCRC Sponsor Contact Form

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