Jr. Clinical Research Coordinator

As the Jr. Clinical Research Coordinator, you will be responsible for coordinating and facilitating the daily activities that play a critical role of the clinical studies according to the protocol, Good Clinical Practices (GCP), Standard Operating Procedures (SOP), and Federal and applicable regulationsReasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Sets up and conducts studies in compliance with the protocol, SOPs, applicable regulations, and GCPs.Prepares, completes, organizes, and maintains all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study-specific documents.Performs station and instrumentation duties on other studies as assigned, including the collection and recording of clinical information.Prepares for and conducts pre-study meetings; assures that staff working on their managed studies understand and are performing duties according to the protocol, SOPs, and GCPs.Reviews and provides feedback on draft protocols, recruiting materials, and draft clinical study reports.Coordinates scheduling subjects for visits and orders checks for subject compensation.Responds to queries from Quality Assurance and Statistics Departments.Prepares and is accountable for all Test Material for managed studies.Adheres to the study budget.Provides excellent customer service to clients and panelists and maintains positive interaction with peers and supervisors.Completes other duties or tasks assigned by the Clinic Manager and/or Supervisor.Adheres to internal standards, policies, and procedures.Performs other duties as assigned.