Employer Industry: Healthcare Services

Why Consider this Job Opportunity:
- Competitive salary up to $85,907 annually
- Opportunity for career advancement and growth within the organization
- Supportive work environment with a focus on professional development
- Comprehensive healthcare benefits for employees and their families
- Generous retirement plans to help you save for the future
- Access to a wide range of wellness and work-life resources

What to Expect (Job Responsibilities):
- Coordinate Phase I-III clinical trials sponsored by the NCI/NCTN
- Prepare and process all initial oversight submissions regulatory documentation
- Resolve regulatory queries and participate in the initiation of new studies
- Participate in regulatory staff meetings and ongoing protocol training
- Organize and maintain all regulatory affairs documentation/files as required

What is Required (Qualifications):
- Bachelor's degree in a life science or human subject protection field
- 5-7 years of research experience
- Effective problem solving and critical thinking abilities
- Knowledge of IRB and human research protection regulations
- Strong organizational and time management skills

How to Stand Out (Preferred Qualifications):
- Experience conducting high-risk biomedical research and/or oncology regulatory research
- Associated research credentialing (CCRP, CIP, etc.)

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