Employer Industry: Higher Education and Research

Why consider this job opportunity:
- Salary up to $50,000 annually
- Comprehensive healthcare and tuition benefits for employees and their families
- Generous retirement plans with a variety of investment options
- Substantial time away from work for personal needs and recovery
- Opportunities for professional development and growth within the institution
- Access to a vibrant urban campus with cultural and recreational activities

What to Expect (Job Responsibilities):
- Coordinate and conduct clinical studies, including subject recruitment, informed consent, chart maintenance, and data entry
- Manage IRB submissions and renewals in compliance with FDA and IRB guidelines
- Ensure protocol compliance and maintain accurate data and documentation
- Oversee study preparation, blood sample processing, and analysis
- Educate patients and family members about clinical study participation

What is Required (Qualifications):
- Bachelor of Science degree
- 1 to 2 years of relevant experience or equivalent combination of education and experience
- Strong understanding of federal regulations and guidance for clinical studies
- Knowledge of good clinical practices
- Ability to work collaboratively with faculty and research teams

How to Stand Out (Preferred Qualifications):
- Experience with database management and analysis
- Familiarity with clinical trial protocols and regulatory requirements
- Strong organizational and problem-solving skills
- Excellent communication skills with the ability to educate participants

#HigherEducation #ClinicalResearch #CareerOpportunity #ProfessionalDevelopment #CompetitiveBenefits

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