Sponsors / CROs
Clinical Research in Seattle, Washington
Seattle Clinical Research Center is dedicated to conducting high-quality clinical research for people of all genders. Since 1993, we have conducted over 300 Phase I, II, III, and IV studies across a range of indications and therapeutic areas. Our clinical trials facility in Seattle, Washington, covers a diverse population of potential patients.
Proven Patient Recruitment Model
Seattle Clinical Research Center has a database of healthy, reliable volunteers actively maintained and developed by our recruitment team. We have the capability to quickly identify and enroll participants into our trials. Knowledgeable recruitment staff provide thorough screening to identify qualified participants and minimize screen fail rates. We maintain a database of nearly 30,000 participants who are eligible for a wide variety of studies.
Experienced Oversight
Our team of doctors, headed by Dr. Ashley Fuller and Dr. Rebecca Dunsmoor-Su, ensures the highest quality standards for every clinical trial. Backed by skilled physicians, ACRP certified research coordinators, assistants, and recruitment specialists, we deliver precise, reliable results in compliance with Good Clinical Practice and CFR/ICH Guidelines at our state-of-the-art Seattle facility.
Proven Record of Success
We pride ourselves on efficiency and excellence. By managing contracts and budgets in-house, we enable rapid study start-up and timeline adherence. Sponsors consistently praise our attention to detail, high-quality results, and ability to meet—and often exceed—enrollment goals.
Reliable Volunteers
Seattle’s vibrant and diverse community embraces research, providing a strong foundation for successful clinical trials. Our recruitment team maintains a robust database of reliable participants, enabling swift identification and enrollment for various studies. With thorough screening and prompt follow-up on referrals within one business day, we ensure low screen-failure rates, high retention, and a smooth study progression.
Areas of Expertise
- Acne
- Contraception
- Dermatology
- Endometriosis
- Female Sexual Dysfunction
- Fibroids
- Heavy Menstrual Bleeding
- Healthy Volunteers
- HPV
- Medical Devices
- Menopause
- Migraines
- Ovulation
- Obesity
- Osteoporosis
- Sleep Medicine
- Urogynocology
- Premenstrual Syndrome
- Vaccines
- Vaginal Atrophy
- Vaginal Infections
- Vasomotor Symptoms
- Weight Loss
Site Capabilities
Our facility is fully equipped to support a wide range of clinical trials with advanced capabilities, including:
- Custom-built 11,500 SF clinic.
- In-house ultrasound, colposcopy, and endometrial biopsy.
- Phlebotomy and PK sample collection and processing.
- State-of-the-art electrocardiogram (ECG) and polysomnography equipment.
- 6 overnight stay rooms for extended studies.
- 6 long stay recliners.
- Full laboratory, including refrigerated centrifuge.
- Trained staff for specimen processing, storage, and shipping.
- Medical grade vaccine fridge with 24/7 temperature monitoring.
- -20 degree C and -80 degree C freezers.
- Specialized infrastructure, including a laminar flow hood and temperature-controlled storage for investigational products and specimens.
- Designated monitor rooms with copy and scanning capabilities.
- 5 private intake rooms and 6 exam rooms designed for patient comfort and efficiency.
- These resources allow us to deliver high-quality data and provide a seamless experience for both participants and sponsors.
Start Up Timelines
Our site's start up timelines can support and optimize your trial's efficiency.
- Contract and Budget Execution: Average completion time of 2–4 weeks.
- IRB Submission: Ready to submit within 2 weeks on average.
- Regulatory Document Preparation: Done concurrently with contract and budget negotiations, saving valuable time.
- Feasibility Questionnaire Completion: Submitted within 3-5 business days on average
