Clinical Research Coordinator: Patient-Focused Trials & Data

Saint Francis Hospital, Inc.; United States; On-site; USD 70,000 - 90,000; Full time

Job summary

Saint Francis Hospital, Inc. in Tulsa, OK is seeking a Clinical Research Coordinator to support multi-disciplinary trials. You will recruit patients, obtain informed consent, and manage data collection and regulatory documentation to ensure timely reporting of adverse events and study results.

The role requires a Bachelor’s degree (CCRP preferred) and 2+ years of clinical research experience, with strong communication and time-management skills in a hospital setting.

Qualifications

• Bachelor’s degree required; CCRP preferred.
• Minimum 2 years of related clinical research experience.
• Working knowledge of medical terminology and healthcare management methodology.
• Ability to use Word, Excel and database programs to produce reports.
• Strong written and verbal communication skills.

Responsibilities

• Recruits and screens clinical research patients for protocol eligibility.
• Obtains informed consent and educates patients on study design, side effects, responsibilities and rights.
• Serves as a resource to physicians regarding protocol requirements and data needs.
• Performs data collection and analysis of test results and records.
• Collects data from physician offices and patient charts for research studies.
• Acts as liaison for patients, families, physicians, and regulatory bodies.
• Coordinates with clinics to assure billing compliance and drug accountability.
• Instructs data analysts to ensure protocol parameters are correctly applied.
• Prepares new study applications and consent forms for IRB approval.

Skills

Clinical research

Informed consent

Data collection

Regulatory documentation

Epic Research Module

Time management

Communication

Education

Bachelor’s degree

Certified Clinical Research Professional (CCRP) (preferred)

Tools

Excel

Access

Word

Job description

Saint Francis Hospital, Inc. in Tulsa, OK is seeking a Clinical Research Coordinator to support multi-disciplinary trials. You will recruit patients, obtain informed consent, and manage data collection and regulatory documentation to ensure timely reporting of adverse events and study results.

The role requires a Bachelor’s degree (CCRP preferred) and 2+ years of clinical research experience, with strong communication and time-management skills in a hospital setting.