Research Coordinator 2

Hours of Work

• 40
• Days
• Of
• Week : 5 Work Shift :

Job Description

• Your Job: In this highly technical, fast-paced, and challenging position, you'll collaborate with multidisciplinary team members to provide the very best care for our patients. The Research Coordinator 2 perform coordination of all phases of the research process. The Responsibilities will include attainment of the approval process required, coordination of data collection, management, patient follow-up and tracking. Your Job Requirements:
• Bachelor degree or Medical Assistant in appropriate discipline
• RN Degree preferred
• Medical Assistant Certification, and/or a Certified Clinical Research Coordinator (CCRC) required
• LVN or RN license, preferred
• 2 or more years of related experience Your Job Responsibilities:
• Available to sponsor monitors upon study site visits
• Follow patients throughout study
• Maintain statistical information
• Following all rules and regulations from the FDA, IRB, and other agencies designated by the sponsors.
• Initiating and maintenance of IRB regulations (including completion of all required documents for submitting for IRB approval)
• Coordinating all phases of assigned clinical trials: Ensuring protocol compliance;
• Collecting, interpreting and reporting all clinical data
• Maintaining drug inventory
• Preparing charts for clinic: Pull charts prior to clinic visit
• Organization of data pertinent to clinic visit
• Completion of case report forms
• Attending regular meetings with physicians and other research staff in order to get updates on the progress of the research studies/patients on treatment
• Track lab results and obtains final result for NP or Physicians to review: Makes sure lab results are received in a timely manner
• Triaging all phone calls for patients (research related or standard of care) considering treatment, on treatment or being followed after treatment