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Employment Type
Full-Time -
Benefits Offered
Dental, Life, Medical, Vision -
Compensation
$50,000 to $65,000 per year
Why Work Here?
Lots of room for growth!
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
• 1 to 2 years of hematology and oncology clinical research experience preferred
• 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
About Renovatio Clinical Consultants LLC:
Renovatio Clinical provides its services to any healthcare clinical entity which includes, but is not limited to, private clinics, for-profit and non-profit organizations whether academic or non-academic, sponsors, and clinical research organizations with a client base primarily comprised of healthcare professionals aspiring to incorporate or already conduct clinical research at their practices.
Since its inception, Renovatio Clinical have proven to be a key strategic clinical research partner to sponsors and clinical research organizations by demonstrating fast clinical trial progress, from as early as protocol review and site selection, through pre-screening patients, contract negotiation and budgeting, completing regulatory paperwork, as well as subject recruitment, enrollment, and retention.
Renovatio Clinical team is comprised of highly qualified research personnel who manage the daily clinical research conduct and operations at its business associates’ sites under principal investigator’s supervision and oversight as defined per Good Clinical Practices guidelines and federal regulations. Renovatio Clinical processes and systems minimize risks of delay in patient enrollment and data acquisition while guaranteeing superior data quality, which leads to trial completion in exceptional timelines with excellent data quality.
Posted date: 5 days ago