Clinical Research Coordinator — Data-Driven Trials

Saint Francis Hospital, Inc.; Bixby (OK); On-site; USD 55,000 - 75,000; Full time

Job summary

Saint Francis Hospital, Inc. in Tulsa, OK seeks a Clinical Research Coordinator to support investigations across multiple disciplines.

You will recruit and screen patients, obtain informed consent, and coordinate data collection, regulatory documentation, and reporting of adverse events under an IREB framework. Ideal candidates hold a Bachelor’s degree (CCRP preferred), with 2+ years of clinical research experience, proficiency in MS Word/Excel/Access, and strong written and verbal

Qualifications

• Bachelor’s degree, preferred.
• CCRP certification preferred.
• Minimum 2 years of related clinical research experience.
• Knowledge of medical terminology and healthcare management.
• Proficiency in Word; working knowledge of Excel and Access for reports.

Responsibilities

• Recruits and screens clinical research patients for protocol eligibility.
• Obtains informed consent and educates patients on study design and responsibilities.
• Serves as a resource to physicians on protocol requirements and data needs.
• Performs data collection and analysis of test results and records.
• Collects data from physician offices and patient charts.
• Acts as liaison for patients, families, physicians, and regulatory representatives.
• Coordinates billing compliance and drug accountability with treatment sites.
• Prepares new study applications and informed consent; submits for IREB approval.

Skills

Verbal communication

Written communication

Data entry

Time management

Attention to detail

Independent work

Team collaboration

Education

Bachelor’s degree

Tools

Word

Excel

Access

Job description

Saint Francis Hospital, Inc. in Tulsa, OK seeks a Clinical Research Coordinator to support investigations across multiple disciplines.

You will recruit and screen patients, obtain informed consent, and coordinate data collection, regulatory documentation, and reporting of adverse events under an IREB framework. Ideal candidates hold a Bachelor’s degree (CCRP preferred), with 2+ years of clinical research experience, proficiency in MS Word/Excel/Access, and strong written and verbal