Research Intern

Please do not call our office - we will reach out to you.DescriptionThe Research Intern is an entry level clinical research position. The Intern will perform a variety of research, database and clerical duties of a routine and technical nature to support clinical trials and assist investigators to organize, gather and compile clinical research data. The Intern will primarily be responsible for the collection, aggregation, and analysis of data. The Research Intern will also form other duties such as data entry, and administrative duties such as filing, record keeping, photocopying, and creating flyers/posters. The Research Intern will be supervised by a senior research staff member or principal investigator.QualificationsMinimum EducationHigh School Diploma or GED (Required) OrBachelor's Degree May require a Bachelor's degree based on the specific internship programMinimum Work Experience0-2 years related experience. 2 years experience working in a medical or scientific research setting, preferredRequired Skills/KnowledgeDemonstrates adherence with the standards for the responsible conduct of research.Work requires organizational skills, knowledge of basic mathematical, data collection and analysis, and research principles.Knowledge of human subjects research.Excellent computer skills in a Windows and/or Mac environment.Excellent writing, editing, and proofing skills.Required Licenses and CertificationsCITI Certification (Required)Valid Driver's licenseFunctional AccountabilitiesResearch ProjectsMaintain confidentiality of data, as required.Plan, conduct and manage research projects.Responsible for appropriate use of research funds and resources.Project AdministrationEnsure compliance with program guidelines and requirements of funding and regulatory agencies.Stay informed of and adhere to human research protection guidelines, relevant best practices, and changes to any research protocol.Accurately complete IRB submissions on time.Anticipate study needs and work to accomplish them in a timely manner.Seek assistance, when needed. Data CollectionCollect data in order to facilitate operational and clinical research activities.Enter clinical and research data and information into database, include electronic CRFs and sample tracking databases.Follow established guidelines in the collection of clinical data and/or administration of clinical studies.Support aggregation and analysis of study data, as directed by senior research staff. Professional DevelopmentAttend and contribute to team meetings, including working to set and achieve project timelines and deliverables.Obtain training and certification as required by study protocol (e.g., CITI training).Comply with all annual job-related training requirements.