Clinical Research Coordinator - Neurology

Baycare Health System•Saint Petersburg, FL

9d•Onsite

About The Position

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 Coordinator - Neurology Facility: St. Anthony's Hospital

Requirements

Clinical Research Coordinator II
Required - Bachelor's degree in related field in lieu of experience
Or - 2 years of research experience with an Associates Degree in related field and CRC (Clinical Research), Radiology License, Cardiology License, RRT/Active NBRC (Respiratory), or CRT/Active NBRC (Respiratory)
Or - 5 years of research experience with a High School Diploma and CCRP (Clinical Research) or CCRC (Clinical Research)
Or - 5 years LPN experience and 1 year coordinator role with a Technical School and LPN License
Or - 2 years LPN and 5 years Research with a Technical School and LPN License
Clinical Research Coordinator III
Required - 5 years research experience with an Associates degree in related field and CRC (Clinical Research), Radiology License, Cardiology License, RRT/Active NBRC (Respiratory), or CRT/Active NBRC (Respiratory)
Or - 7 years research experience with a Technical School and LPN License
Or - 2 years research experience with a Bachelor's degree in a related field

Responsibilities

Lead and implement clinical trials under the direction of the Principle Investigator in accordance with the standards of good clinical practice, federal and state regulations and institutional review board (IRB) requirements.
Facilitate protocol development
Complete trial feasibility
Ensure study start-up completion worksheet is complete with required protocol specific training of research staff and ancillary departments
Ensure 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 including biometric data and specimen collection
Creation and completion of source worksheets
Building and maintaining EDC systems
Collecting source data for electronic data capture (EDC) systems
Building and completing Case Report Form (CRF)s
Assess patients for trial-related and non-trial related symptoms
Reporting of adverse events
Serious adverse events
Dispensing/accountability of investigational product
Participate in additional business activities to recruit new trials or meet recruitment goal
Mentors new team members to protocol and site processes
Must work independently and use sound judgment while performing job duties.
Perform duties as assigned under the scope of related certification or licensure.