Clinical Research Nurse (*on site position - no remote)*

Sarasota Memorial Health Care System; Sarasota (FL); Remote; USD 60,000 - 80,000; Full time

Job summary

A leading healthcare provider in Sarasota, Florida, is seeking a Clinical Research Coordinator to manage clinical trials. You will ensure compliance with FDA regulations and collaborate with various stakeholders to facilitate research. A BSN and BLS certification are required, along with a commitment to learning Clinical Research practices. This onsite position offers a chance for career growth in a supportive environment.

Benefits

Opportunity for career advancement

Required training for certifications

Collaborative work environment

Qualifications

• Graduate of an accredited school of nursing or a diploma program; BSN required for new hires after 2012.
• Certification as a Clinical Research Coordinator required within one year of eligibility.
• Training in Human Subject Protection and Safe Shipping/Handling of Bio-Hazardous Specimens must be completed within 30 days of hire.
• Valid driver's license and ability to travel to off-site locations.
• BLS certification (Basic Life Support/CPR) is necessary.

Responsibilities

• Coordinate and conduct clinical trials in accordance with good clinical practices and FDA regulations.
• Work under the direction of the Principal Investigator and Manager/Director.
• Ensure compliance with Human Subject Protection protocols.
• Collaborate with staff, subjects, families, and physicians to facilitate clinical trials.
• Maintain accurate documentation and reporting for clinical research activities.

Skills

Clinical Research

Interpersonal Skills

BLS Certification

Education

BSN

Job description

Overview

Employer Industry: Clinical Research

Why consider this job opportunity

• Opportunity for career advancement and growth within a state-of-the-art research institute
• Onsite position with a focus on clinical trials and research
• Engaging and collaborative work environment
• Chance to contribute to meaningful clinical research and patient care
• Required training provided for certifications and compliance

Responsibilities

• Coordinate and conduct clinical trials in accordance with good clinical practices and FDA regulations
• Work under the direction of the Principal Investigator and Manager/Director
• Ensure compliance with Human Subject Protection protocols and bio-hazardous specimen handling
• Collaborate with staff, subjects, families, and physicians to facilitate clinical trials
• Maintain accurate documentation and reporting for clinical research activities

Qualifications

• Graduate of an accredited school of nursing or a diploma program; BSN required for new hires after 2012
• Certification as a Clinical Research Coordinator required within one year of eligibility
• Training in Human Subject Protection and Safe Shipping/Handling of Bio-Hazardous Specimens must be completed within 30 days of hire
• Valid driver's license and ability to travel to off-site locations
• BLS certification (Basic Life Support/CPR)

How to Stand Out (Preferred Qualifications)

• Knowledge of commonly used computer applications
• Experience in clinical research and/or a medical/surgical or critical care setting
• Ability to initiate work without supervision
• Demonstrated proficiency in interpersonal skills with diverse stakeholders

#ClinicalResearch #HealthcareJobs #CareerOpportunity #ClinicalTrials #NursingJobs

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