Location: Remote (up to 40% travel required)
Job Description:
Client is looking for Jr and Sr level CRA’s who are interested in working on several post approval device studies. Client needs candidates who have at least 3 years of Class III Medical device experience, specifically experience in the Neurovascular or Cardiac areas. Need candidates who have strong start-up experience, as some of these sites are starting from the ground up all the way through site initiation. Candidates must come with site initiation and activation experience, experience with contract negotiations, IRB informed consent reviews, and monitoring experience (onsite and remote monitoring). Candidates who have experience handling multiple trials at the same time is preferred as well as Veeva Vault experience. EDC System they use is Zelta-Merative-IBM so experience there is a PLUS, but its easy to learn as long as the candidate has experience with other EDC systems. Last but not least, looking for candidates who have good experience monitoring IDE or FDA mandated post-approval studies (this is a MUST).
Skills:
CRA, Site Monitoring, Site Activation/Site Initiation, Contract/Budget Negotiation, EDC, Neuro and/or Cardiovascular/Cardiac, Medical Device, IDE
Education:
Experience outweighs degree requirement but prefer a B.S. in relevant area.
Remote: CRA’s (5) (233220)
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