Precept Life Sciences is seeking experienced Regional CRAs across the country for permanent positions with several leading CROs.
On average, CRAs are assigned to an average of 12 sites across 1-3 protocols. Study and site assignment will vary depending on monitoring duration/frequency, location of sites and complexity of trial.
CRAs are expected to be 80% billable, with approx. 60% travel.
We are looking for CRAs that are not just field monitors, but those that manage all aspects of the site ...
CRAs - Join Covance and receive a $5000 Sign On Bonus!
Meet the CRA hiring team at the ACRP conference - email [email removed].
Set yourself up for SUCCESS with Early Clinical Development!
Now is the time to join our growing business where you have supportive management and a cohesive team.
At Covance, you are not just a number. We value you and your hard work...we want you to succeed.
URGENT Need for Oncology Monitors! Calling all Experienced Clinical Research Associates / CRAs / ...
A medical diagnostic company is seeking a Director, Clinical Research to join their team in the Seattle, WA area. This is a full-time position and must be office-based (company will assist with relocation).
They are looking for candidates with the following experience:
• They would prefer this person to have an MD degree; however they will consider someone with a PhD or Masters
• Oncology and/or Diagnostics experience is desired
• 10+ years of experience in medical device or pharmaceutical ...
~~I am currently working with a diagnostic company actively seeking a Director of Clinical Research. This position is full time in Seattle, WA.
The client is looking for someone with the following experience:
•Master’s degree, PhD and/or MD.
•10+ years of experience in medical device and/or pharmaceutical experience
•Experience writing, reviewing, and editing protocols and study reports.
•Knowledge of GCP
•Experience interacting with the FDA.
Please let me know if you or anyone you may know if ...
We are currently looking to hire Permanent Regional CRAs
The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, ...
Mar 21 -
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