We're delighted to introduce this AD CDM opportunity with a fast-growing oncology focused biotech based in the Seattle area. Our client is the US based enterprise of a Chinese pharma giant. Their mission is to develop novel therapeutics for various "undruggable" oncology indications, and so far they've made INCREDIBLE progress... Over thirty open studies.
Yes, you read that right. 3-0.
These studies are testing what I call the msot "market appropriate" candidates for oncology indications: ADC's. Time and time again these have proven to be not just safer and more effective than their counterparts, but ultimately cheaper to make, resulting a better cost for the consumer.
This role will report only to the functional head, and will oversee all clinical data activities both stateside in an outsourced model and overseas within an in-house model (team of 20+ CDM's). Lastly, this position will be pivotal for the upcoming submission for their lead candidate, which has been slated for later this year. Additional requisites for this role are as follows:
- Will Report to the VP of Biometrics
- Must be able to go on-site in Redmond, WA
- Must be fluent in Mandarin
- Need to have extensive experience in CRO oversight
- Hands-On Experience in end-to-end CDM experience (start up to close out/ database lock)
- Familiarity with FDA interaction and Submission Process is a major plus
- Needs to be open to management (both direct and dotted line)
- Experience in Data Review, Data Migrations, Edit-Checks, and UAT's is essential
For further information about this position please apply. We look forwad to discussing with you!
