Clinical Research Coordinator II
Screens patients for eligibility in participation of research protocol
Consents patients, and interviews patients to collect data on health history and lifestyle practices
Performs sample collection, processing, and tracking
Prepares samples for shipment, enters the required data, and prepares reports as needed
Participates in routine (weekly / monthly) update calls with client
Responsible for implementing SOPs, research protocols and policies for all assigned research projects
Assists with regulatory submissions and actions
Adheres to legal, professional, and ethical codes with respect to confidentiality and privacy
Assures that protocol requirements are achieved within good clinical practices
Assists with monitoring audits / visits for protocols
Collects, organizes, and maintains appropriate files of data
Maintains status reports on all patients
Performs other duties and responsibilities as assigned or directed by the supervisor
Qualifications
Must have 2-2 years of Clinical Research Coordinator experience
Bachelor's Degree
Knowledge of federal and local regulations and policies pertinent to research involving human subjects
Security Requirement : Ability to obtain and maintain a T3 Secret Clearance
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