Renovatio Clinical is seeking a Clinical Research Coordinator (CRC) with experience in clinical research. CRC will be responsible for the overall coordination and organization of research studies in compliance with study protocol, SOPs, and state and federal regulations. The Research Coordinator will be expected to maintain open, clear, and effective communication with the physician-teams, patients, study sponsors, and internal management.
Minimum Job qualifications:
• Registered Nurse (preferred) or BA/BS in Biomedical Science, Biology, Chemistry, Biochemistry or other life science
• Research certification (ACRP or CCRP) preferred
• 3 years of clinical research experience
• Coordinate protocol related research procedures, study visits, and initiating informed consent process and maintaining source documents
• Screen, recruit, and enroll patients/research participants
• Communicate with laboratories or investigators regarding laboratory findings
• Maintain study source documents and record all necessary research visit notes
• Report adverse events as required per protocol
• Understanding good clinical practice (GCP) and regulatory compliance
• Educate subjects on protocol, study intervention, study drug, etc.
• Good understanding of clinical research and phases I-IV clinical trials
• Practical knowledge of GCP, ICH guidelines, and FDA regulations
