Jobs

Description

MAX bill Rate: $76 Duration: 6 months - until September Location: remote Working Hours: 8-5 or 9 or 9-5 in their time zone Interview Process: 1 hour teams call with HM MUST HAVE: -study start up lead -IRB submissions -vendor management -site start up able to jump in with minimal training 3-5 years of experience Bachelors Degree minimum The position is remote, temporary (6 months), and will end once the current team member returns from leave; it will not convert to a full-time role -The candidate must be able to work standard US business hours in any time zone The person will manage a set list of study sites—some with ongoing start-up, some brand new—responsible for all regulatory document collection and coordination at each site (including IRB/ethics committee submissions) -Must handle vendor management: engage vendors, coordinate site training with systems, and arrange start dates for vendors -Experience as a Study Startup Lead is highly valued; the more experience in this area the better -Technical skills required include IRB submissions and packet preparation, essential document collection, and any site or study startup tasks -Must be able to operate independently with almost no guidance after initial system training; immediate ability to contribute is needed Education: Bachelor’s degree required; master’s or higher not necessary Ideal experience: 3-5 years, but flexible if a candidate is otherwise a good fit Must haves -Study Startup Lead experience -IRB submissions and essential regulatory document management/collection -Vendor management for study and site startup -Ability to work independently with minimal guidance -Team-oriented attitude and willingness to help out broadly -Bachelor’s degree Providing Study Start-up coverage while a team member is out on maternity leave. Primarily responsible for coordinating the study start-up for in-house clinical trials. Works as part of a clinical delivery team providing support, guidance and advice on a local level. Develops existing tools and processes to identify areas of improvement and ensures business continuity for study delivery. Able to solve complex problems within a range of studies. A self-starter who is able to navigate study start-up for multiple clinical trials independently.