Employer Industry: Clinical Research

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- On-site position, fostering collaboration and team engagement
- Supportive and collaborative work environment
- Chance to make a significant contribution to clinical trials and patient care
- Required certifications and training provided to enhance professional development

What to Expect (Job Responsibilities):
- Coordinate and conduct clinical trials under the direction of the Principal Investigator and Manager/Director
- Ensure compliance with good clinical practice standards and FDA regulations
- Drive to off-site locations as needed for trial-related activities
- Maintain accurate documentation and reporting for clinical studies
- Facilitate communication between staff, subjects, families, and other stakeholders involved in clinical trials

What is Required (Qualifications):
- Graduate of an accredited school of nursing or a diploma program; BSN required for new hires after 2012 within specified timeframe
- Certification as a Clinical Research Coordinator within one (1) year of eligibility
- Training in Human Subject Protection and Safe Shipping/Handling of Bio-Hazardous Specimens must be completed within thirty (30) days of hire
- Valid driver's license and ability to drive to off-site locations
- Basic Life Support (BLS) certification required

How to Stand Out (Preferred Qualifications):
- Knowledge of commonly used computer applications
- Experience in a clinical research and/or medical/surgical or critical care setting
- Ability to initiate work without supervision
- Demonstrated proficiency in interpersonal skills with staff, subjects, families, physicians, and sponsors/auditors of clinical trials

#ClinicalResearch #HealthcareProfessionals #CareerOpportunity #ProfessionalDevelopment #ClinicalTrials

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