Identifies patients who are potentially eligible to enroll in the study by reviewing their information in patient lists and in the electronic medical record
Conducts telephone interviews and performs procedures to screen and enroll study participants including obtaining informed consent
Schedules patients for study visits
Utilizes study specific data collection and data documentation tools, completes clinical research assessments, and makes study related observations
Collects and organize patient data
Review data for quality and completeness based on established protocols
Assists with the coordination of the collection, processing, organization, and storage of biological specimens in the systems
May be responsible for IRB and regulatory submissions and maintenance of regulatory files
Maintains ongoing communications with the research coordinator and PIs for data collection needs
Adheres to Good Clinical Procedures (GCP) and Standard Operating Procedures (SOP) as well as to protocol requirements to ensure validity of clinical research patient data
Other duties including send out mailings, taking inventory/ordering supplies, monitoring and setting up equipment
Requirements
Bachelor’s Degree Required
0-2 years of experience
Excellent organization and communications skills required
Strong interpersonal skills; ability to effectively interact with all levels of staff and external contacts
Must be detail oriented and have the ability to follow through
Ability to effectively manage time and prioritize workload
Must practice discretion and adhere to hospital confidentiality guidelines at all times
Must have computer skills including the use of Microsoft Office Suite
Benefits
Professional development
Flexible work arrangements
Job title
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