Clinical Research Coordinator

Responsibilities

• Meets with study participants.
• Follows study protocol performing duties/testing/data collection.
• Conducts study required tests and procedures (e.g., bone density scans, EKG's, balance testing, mental and physical assessments, blood draws, vitals, diary instruction and review).
• Records data into patient research case report forms (CRF's) to include recording test results and reacting appropriately to abnormal results.
• Maintains accurate CRF's and source documents.
• Schedules appointments for various procedures inside and outside the department.
• Obtains medical records for any research hospitalizations and various other duties assigned.
• Maintains study drug and supply inventory as well as study drug disbursement.
• Reports regulatory and Institutional Review Board issues appropriately (e.g., reports adverse events and other regulatory data).

Qualifications

• Bachelor's Degree in related field of science preferred.
• 4 years clinical experience preferably in a research setting.
• Knowledge of FDA regulatory requirements is required.
• Knowledge of the principles of research design.
• Ability to maintain confidentiality.
• Ability to operate personal computer and various software packages.