Careers
At Spiration®, we pride ourselves on our scientific expertise and cutting-edge technologies. We are always on the lookout for experienced professionals who are energetic, committed and passionate about what they do.
Spiration provides dynamic career opportunities, competitive compensation and benefits programs, and a great location in the Pacific Northwest. If you are interested in an environment where teamwork and commitment to excellence are rewarded, check out our current open positions.
If your talents and background fit the positions listed, please forward your resume to:
humanresources@spiration.com
Tel: 425.497.1700 x101
Fax: 425.216.0847
Spiration, Inc.
Attn: Human Resources
6675 185th AVE NE
Redmond, WA. 98052
Spiration, Inc. is an equal opportunity employer and makes employment decisions on the basis of merit. We strive to place the best available people in every job. Spiration is committed to complying with all applicable laws providing equal employment opportunities to individuals regardless of race, color, creed, sex, marital status, age, national origin, sexual orientation, physical handicap, disability, medical conditions or ancestry. This commitment applies to all persons involved in the operations of the company and prohibits unlawful discrimination by any employee of the Company, including supervisors and co-workers.
Current Openings
- Senior Clinical Research Associate |
Download (MS Word)
The Company is seeking a Senior Clinical Research Associate to coordinate and manage clinical trials for the IBV® Valve System, a minimally invasive device under investigation in the U.S. for the treatment of severe emphysema. The system has received CE Mark approval for the treatment of diseased and damaged lung in Europe and is an investigational device in Canada.
This individual will be part of an interdisciplinary team coordinating all clinical study activities, and will:
- Participate in site qualification and initiation process.
- Assist clinical sites to ensure timely subject screening and enrollment.
- Manage distribution, collection and tracking of regulatory documentation for clinical sites to ensure compliance at clinical sites and Sponsor’s Central File.
- Monitor clinical studies for protocol compliance, coordinate day-to-day activities of trial sites.
- Assist in planning, preparing, and distributing materials for investigator and coordinator meetings and for study-related training.
- Track and report progress of studies including patient enrollment/screening, data collection, and adverse event documentation.
- Assist in query writing and resolution process, as required. Identify and gather missing or incomplete data from clinical sites.
- Assist with the development and implementation of corrective actions for addressing noncompliance issues at individual sites.
- Act as company liaison, working with clinical sites to resolve any site related issues quickly and effectively.
- Conduct site visits as necessary. Must be able to travel 30%-40%
The ideal candidate will:
- Thrive in an early-stage company atmosphere, working with engaged peers dedicated to success.
- Have a Bachelors degree in a life science or medical discipline; R.N. preferred. (Appropriate, relevant on-the-job experience may be substituted for minimum educational requirement)
- Have at least five years year’s clinical research experience including, two and a half years monitoring clinical trials.
- Possess a thorough knowledge of Good Clinical Practices (GCPs), device life cycle, and clinical monitoring procedures.
- Demonstrate a team player attitude and willingness to contribute along with everyone else