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

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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


Qualifications:

• 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: hr@impelneuropharma.com

• Location: Seattle, Seattle, WA

• Post ID: 60886027 seattle
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