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Posted: Tuesday, February 20, 2018 12:08 AM


Job Description:

The Clinical Trial Associate will provide support for all clinical activities, ensuring the successful completion of clinical trials.

Responsibilities include the following. Other duties may be assigned.

• Track and manage CRFs, queries and clinical data flow. May act as central contact for the clinical team for designated project communication, correspondence and associated documentation
• Prepare, handle and distribute Clinical Trial supplies and maintenance of tracking information
• Participate in team meetings and generate meeting agendas and minutes
• Assist with the entry and tracking of data/samples in clinical databases and other associated data tracking tools
• Maintain databases for appropriate study administration
• Prepare and perform periodic review of the TMF including all GCP-related documents
• Administer all study and related documents (correspondence, monitoring reports, contact reports, and other organizational documents) before and during the study
• Coordinate with external vendors and sites
• Generated/Track Check Requests for Investigator, Vendor Payments, and Pass Thru • Payments based on the requests received by PM and/or Clinical Operations Manager


• Bachelor’s Degree or higher in a relevant field
• 1-2 years of experience in pharmaceutical industry or CRO
• Experience supporting clinical trials
• Basic knowledge of drug development and FDA GCP regulatory guidelines
• Excellent oral and written communication, with particular attention to detail
• Excellent organizational and problem-solving skills
• Proven ability to learn and adapt in an evolving work environment
• Advanced-level proficiency with MS Word, Excel, and Adobe Acrobat
• Familiarity with MS project, MS Visio applications is preferred

Qualified candidates, please email your resumes to:

• Location: Seattle, Seattle, WA

• Post ID: 60886027 seattle is an interactive computer service that enables access by multiple users and should not be treated as the publisher or speaker of any information provided by another information content provider. © 2018