Duration:
6 months (potential extension or opportunity to convert)
Job Description:
Our client is currently seeking an experienced CTM to assist the current CTM with hands-on support for a series of IVD programs. The protocols are in motion and the resource would be assisting the existing CTM with additional support surrounding site ramp up, site training, project management, enrollment initiatives, contribute to user acceptance testing processes and coordination with lab for sample procurement activities. The studies are focused on diabetics and kidney failure and IVD products and good portion of this contract will also cover project management functions such as managing/setting timelines, follow-ups, etc. Additional responsibilities will include paired sampling, patient recruitment, patient population, sample procurement and patient identification. There are three existing sites with intent to add additional sites, however there is a significant emphasis on sample procurement, patient identification, project management throughout trials, and overall site management & monitoring efforts.
Experience with in-house CTM experience in either pharma or within a bigger CRO and at least 5-10 years of experience with the functions listed above. This is a hands-on role that will require an appropriate degree or sense of professional urgency, with a go-getter aptitude, attention-to-detail and prospective thinking. IVD expertise preferred.
Bonus/Nice to have (not required):
CCRA, PMP certification
Remote: Clinical Trial Manager (233828)
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