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Clinical Research Registered Nurse

Req #: 17006701
Location: Tampa, FL
Job Category: Research
Organization: Florida Hospital Tampa

Description

Work Hours/Shift

FT Days

 

Florida Hospital Tampa

Our hospital has celebrated many firsts in Tampa’s health care history since we opened our doors in 1968. Today, more than four decades later, Florida Hospital Tampa continues to offer innovative medicine as we elevate health care in the Tampa Bay region.

 

At Florida Hospital Tampa, our diverse clinical specialties provide world-class health care to our patients. We offer the most trusted, expert care in key specialties including cardiovascular care, neurosciences, orthopedics, women's health, cancer and surgery. Our skilled surgeons not only utilize minimally invasive and robot-assisted procedures, but they are also leaders in improving these advanced techniques.

 

You will be responsible for:

  • Coordination and planning of budgets, people and time management
  • Protocol evaluation and feasibility including budget evaluation
  • Clinical trial preparation involving the planning, assembling and instruction of the trial team, development and evaluation of patient information and informed consent forms and patient recruitment
  • Regulatory and ethical submissions and procedures and communicating with relevant authorities
  • Implementation of the clinical trial from initiation through the stages of development documents, SOPs, tools, organization facilities and licenses
  • Recruitment and co-ordination of the trial subjects covering informed consent, screening and inclusion of the subjects adhering to safety and compliance issues
  • Co-ordination and management of the clinical trial, communication with sponsor and authorities, visit coordination, sampling, time management and product accountability
  • Data collection and management, collection of source documents, using and developing CRFs, registration and management AEs, filing and archiving, managing monitoring visits, dealing with queries
  • Close-out of the clinical trial, contributing to research article, audit preparation, trial closure, communication with authorities and other disciplines involved, assisting in the final study report and completing financial obligations.
Qualifications

 

What will you need?

  • Demonstrates relevant skills to be successful in a research environment. 
  • Demonstrated excellent team working skills with ability to work using own initiative. Effective listening and interpersonal skills. Time management skills/ability to prioritize workload.
  • IT skills.
  • Proactive attitude Open and clear communicator. Understands the needs of others. Recognize potential obstacles and work to resolve them within set timelines. Conscientious and precise delivery of work even when under pressure
  • Flexible and open to change.
  • Evidence of further education including post-graduate certification / diploma / continuous professional development in a relevant area. Demonstrated excellent team working skills with ability to work using own initiative. (Preferred)
  • Graduate from an accredited school of Nursing
  • Related experience demonstrating the appropriate competencies and skills for the job and clinical setting.
  • Research experience including awareness of FDA / OHRP / ICH / GCP Guidelines and relevant state and federal regulatory/statutory guidelines.
  • Master’s degree in a health related field (Preferred)
  • 2 years clinical research experience. (Preferred)
  • Cardiology experience preferred (Preferred)
  • Current registration with Florida State Board of Nursing as a registered professional nurse or licensure from another state with verification of application and eligibility for Florida licensure by endorsement.
  • Certification by ACRP or SoCRA or obtain within 3 years of hire.

 


This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.
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