Clinical Research Nurse

Job summary

Coordinates and implements clinical research studies, ensuring compliance with study protocols, good clinical practice, regulations, and institutional review board requirements. Manages participant scheduling, recruitment, consent, regulatory documentation, data collection, clinical follow-up, adverse event reporting, and investigational product accountability.

Job details

Join the team that is revolutionizing health care – BayCare Health System Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that’s built on a foundation of trust, dignity, respect, responsibility, and clinical excellence. Title: Clinical Research Nurse Facility: St. Joseph's Hospital Responsibilities Coordinates and implements research studies for assigned services under the direction of the Principal investigator in accordance with the standards of good clinical practice, federal and state regulations and institutional review board (IRB) requirements Ensures adherence to the study protocol and schedule of events Patient visit scheduling for protocol related procedures Screening, study recruitment, preparation of IRB reports Establishment and maintenance of regulatory documents Performing the process of informed consent and HIPPA authorization Clinical follow-up of study subjects Creation and completion of source worksheets, Collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF) completion Assesses patients for trial-related and non-trial related symptoms Reporting of adverse events, serious adverse events, and dispensing / accountability of investigational product Must work independently and use sound judgment while performing job duties Performs duties as assigned under the scope of related certification or licensure BayCare Offers a Competitive Total Reward Package Including Benefits (Medical, Dental, Vision) Paid Time Off Tuition Assistance 401K Match and additional yearly contribution Annual performance appraisals and team award bonus Family resources and wellness opportunities Community perks and discounts Certification Required RN (Registered Nurse) Preferred CCRC (Clinical Research) Education Required Associates in Nursing Or - Diploma in Nursing Preferred Bachelor's in Nursing Experience Required 2 years healthcare or management Preferred Clinical Research experience Location: Tampa, FL Status: Full Time, Exempt: Yes Shift Hours: 8:00AM - 4:30PM Weekend Work: None Equal Opportunity Employer Veterans/Disabled

What you’ll do

Coordinates and implements clinical research studies, ensuring compliance with study protocols, good clinical practice, regulations, and institutional review board requirements. Manages participant scheduling, recruitment, consent, regulatory documentation, data collection, clinical follow-up, adverse event reporting, and investigational product accountability.

Requirements

An associate degree or diploma in nursing is required, and a bachelor's degree in nursing is preferred. An active Registered Nurse certification is required; two years of healthcare or management experience is required, while clinical research experience and Clinical Research Coordinator certification are preferred.

Benefits

• Medical Insurance
• Dental Insurance
• Vision Insurance
• Paid Time Off
• Tuition Assistance
• 401(k) Match
• Additional Yearly 401(k) Contribution
• Annual Performance Appraisals
• Team Award Bonus
• Family Resources
• Wellness Opportunities
• Community Perks and Discounts

Listed skills

• Recruitment · Preferred
• preparation · Preferred
• Health · Preferred
• responsibility · Preferred
• Compliance · Preferred
• management · Preferred
• Process · Preferred
• Documentation · Preferred
• Reporting · Preferred
• Time · Preferred
• maintenance · Preferred
• scheduling · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Clinical Research Coordination
• Good Clinical Practice
• Research Protocol Compliance
• Patient Scheduling
• Patient Screening
• Study Recruitment
• Informed Consent
• HIPAA Authorization
• Regulatory Document Management
• Institutional Review Board Reporting
• Clinical Follow-Up
• Source Data Collection
• Electronic Data Capture
• Case Report Form Completion
• Adverse Event Reporting
• Investigational Product Accountability

Job areas

• Healthcare
• Science & Research

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