Clinical Research Coordinator

The Clinical Research Coordinator plays a crucial role in managing clinical trials and research studies related to oncology. This position will also help the clinic to design workflows and monitor the GPRA quality measures.  This position works closely with the Medical Director, providers, researchers, regulatory bodies, and patients to ensure that clinical trials are conducted effectively, ethically, and in compliance with regulatory standards. This study coordinator will also work with the clinic and community in improving health outcomes including, but not limited to cancer screening, tobacco cessation, improvement of health quality metrics.

This list is intended only to illustrate the various types of work that may be performed.  The omission of specific statements does not exclude them from the position if the work is similar, related or is a logical assignment to the position.

Required: Bachelor's degree or equivalent experience, Minimum two to three years' experience in a clinical research or cancer registry environment with regulatory or human research protections

Preferred:

• Minimum five years of experience in a research environment with regulatory or human research protections.
• Experience working with Electronic Health records and Clinic Trial Management system.
•  Knowledge of clinical trials records, procedures, and computerized data processing systems.
• Ability to work with multiple data management systems including generating reports and sourcing data from systems. 
• Knowledge of RPMS and EPIC EHR systems.
• Ability to extract data from medical records. 

Skilled In:

• Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
• Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
• Proficiency is Microsoft Excel, including data entry, formatting and creating charts and tables.

Knowledge of:

• Knowledge of clinical trials records, procedures, and computerized data processing systems.
• Knowledge of how to synthesis study conduct.

Ability to:

• Ability to work with multiple data management systems including generating reports and sourcing data from systems.
• Ability to extract data from medical records
• Ability to apply judgement in interpreting regulations, determining impacts, and knowing when to escalate questions and concerns when appropriate.
• Ability to develop and/or present content to internal team and external groups

The working conditions described here are representative of those that must be met by an employee to successfully perform the essential duties of this class.  

 While performing the duties of this job, the employee is frequently required to sit and talk or hear.  The employee is occasionally required to walk; use hands to operate, finger, handle, or feel objects, tools, or controls; and reach with hands and arms.  The employee must occasionally lift and/or move up to 30 pounds.  Specific vision abilities required by this job include close vision and the ability to adjust focus.  The noise level in the work environment is usually moderately quiet