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Intern - Clinical Research
3 months ago
JOB SUMMARY
ExperienceTypically requires a minimum of 2 years of experience. Less that than 2 years experience and student interns will be considered.KnowledgeRequires basic job knowledge of systems and procedures obtained through prior work experience or education.EducationHigh School Diploma or equivalentAdditional Work Experience3 years administrative support experienceOrEquivalent combination of education, training and experience
RESPONSIBILITIES
• Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
• Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness.
• Assist CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.
• May perform assigned administrative tasks to support team members with clinical trial execution.
REQUIRED SKILLS
Performance monitoring and evaluation, Project management, Reporting, Ability to coordinate, Documentation and record keeping
REQUIRED EDUCATION
Bachelor's degree
