Job Description:Looking to hire an individual with aclinical researchbackground to act as a consultantCRCto support am ongoing clinical trial.
The main job duties for this position will be regulatory filing, creating source documents, data entry (EDC), along with patient recruitment and other research administrative duties.*This role requires research experience*Duties and ResponsibilitiesRegulatory Filling and SubmissionsConsentingData Entry/ManagementCollection of study data and entering data intoEDC(as well as keepEDCup to date)Creating source documentsChart review/phone screeningStudy administrationAny study efforts deemed necessary by siteRequirements:Clinical Research ExperienceHighly independentWilling to obtain Good Clinical Practices (GCP) certifiedExperience in study start up (preferred)*This position isnotremote*Recruiter: ShelbyCiardelli(763) 923-2058 About Actalent:Actalent connects passion with purpose.
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