Under limited supervision, the Clinical Research Coordinator I (CRC) coordinates patient care in compliance with local, state and federal guidelines and regulations through IRB approved protocol requirements.  The CRC uses their developing and/or basic knowledge of clinical trial research along with their hospital experience to work collaboratively with individuals associated with the care and treatment of the patient. It is the expectation the CRC will utilize day-to-day experience and collaborations with senior staff to broaden their knowledge base and capabilities.  They will seek out opportunities to build their knowledge of the organization, research processes and scope of work.  They will understand the guidelines, regulations, and policies associated with conducting clinical trial research and use that insight to evaluate and resolve problems or seek out guidance.  The CRC collaborates with the investigators, research staff and other departmental stakeholders to conduct clinical trial coordination per protocol.  Through clear documentation, the CRC will define any changes in condition, adverse events, concomitant medication use, protocol compliance, and response to study intervention.  The CRC works collaboratively with individuals associated with the care and treatment of the patient.

Qualifications:

• Technical Diploma or Degree/certification must be in biology, public health, pharmacy, or health related field.

• Oncology clinical experience, not required, but preferred for this role.

• 3 years of experience in clinical research or as a clinical trial coordinator.

• Proficient with a computer including navigating websites, electronic data systems, electronic medical records, Excel, Word, PowerPoint.

• Must obtain ACLS/BLS training within 6 months