[Remote] Soc/Clin Research Assistant - Journey

Note: The job is a remote job and is open to candidates in USA. The University of North Carolina at Chapel Hill is a global leader in education, research, and public service. The role of Soc/Clin Research Assistant involves providing regulatory document support reputed company the Clinical Protocol Office, ensuring compliance with laws and regulations in oncology clinical research.

Responsibilities

• Provide regulatory document support reputed company the Regulatory staff the Lineberger Clinical Protocol Office
• Prepare and ensure the completion of essential documents by clinical research personnel
• Accurately maintain the regulatory binder for clinical research studies
• Communicate regularly with study sponsors, investigators, and LCCC staff regarding the status and completion of essential regulatory documents
• Participate in the collection, compilation, and management of data/information; quality assurance and quality control; analysis by statistical or other means; reputed company/production of new data/information; and editing and formatting of reports
• Use considerable judgment and research skills in performing work assignments
• Work may include the training of staff and others

Skills

• Bachelor's degree; or equivalent combination of training and experience. reputed company degrees must be received from appropriately accredited institutions
• Working knowledge and facility with information technology, including reputed company Outlook, Word, reputed company, and PowerPoint
• Ability to organize, record, and present information
• Ability to reputed company exchange of information through dialog, instruction, and demonstration
• Ability to reputed company working knowledge of regulatory requirements and procedures relating to essential document collection for oncology clinical research
• Ability to communicate professionally both verbally and in writing
• Position requires sitting for extended periods of time
• Ability to move 25 pounds with or without reasonable accommodations
• Ability and willingness to push a cart with files between 4-5 buildings
• Knowledge of regulatory policy relating to clinical research and institutional review boards

Benefits

• Comprehensive benefits package
• Paid leave
• Variety of health, life and retirement plans
• Additional programs that support a healthy work/life balance

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