Senior Clinical Research Associate (Mounds View)
Occupations:
Clinical Research CoordinatorsClinical Data ManagersMedical Scientists, Except EpidemiologistsRegistered NursesNatural Sciences ManagersIndustries:
Offices of PhysiciansNursing Care Facilities (Skilled Nursing Facilities)Junior CollegesSpecialty (except Psychiatric and Substance Abuse) HospitalsOther Professional, Scientific, and Technical ServicesTitle: Clinical Research SpecLocation: Mounds View, MNDuration: 24 Months+ Possible ExtensionMust Have:Experience with CTMS and patient data and site management systems (i.e. Veeva Vault, RAD Rave, Oracle).Experience with Microsoft Office Applications.HM's Top Needs:Site Management experience (site or sponsor)Knowledge of/experience with CTSM/EDC/TMFExperience with Good Clinical Practice (GCP)Something nice to have, but not necessary: Experience with DiabetesEducation Required: Bachelor's degree (preferred degree in life sciences or medical/scientific field).Years' Experience Required: Minimum 2 years with bachelor's degree and 0 years' experience with advanced degreeJob Duties:Oversees, designs, plans and develops clinical evaluation research studies.Prepares and authors protocols and patient record forms.Conducts registered and nonregistered clinical studies of products that have been determined to satisfy a medical need and/or offer commercial potential.Oversees and interpret results of clinical investigations in preparation for new drug devices or consumer applications.Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets.May be responsible for clinical supply operations, site and vendor selection.