What are the responsibilities and job description for the Clinical Research Coordinator position at SFI Independence, Ohio?
We are seeking a Clinical Research Coordinator to join our team!
This role establishes and executes all logistics related to a variety of clinical research projects - including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. The successful candidate will coordinate all administrative functions for research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE’s and source documents.
Responsibilities:
- Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process.
- Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution of queries from sponsors or regulatory entities.
- Coordinates institutional, pharmaceutical and internal audits, including facilitating third party study monitoring and designs and implements needed corrective actions.
- Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
- Responsible for timely submission of adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
- Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality.
Qualifications:
- 3 years of Clinical Research Experience
- Associate Degree/Bachelors or higher preferred
- SoCRA or ACRP Certification
- Experience with Oncology Setting
Salary : $26 - $35
