Employer Industry: Cancer Research and Clinical Trials

Why consider this job opportunity:
- Opportunity for career advancement and growth within a prestigious cancer research institution
- Work remotely, providing flexibility in your work environment
- Be part of a dedicated team at one of only 50 designated comprehensive cancer centers in the nation
- Engage in meaningful work that contributes to cancer prevention, diagnosis, and therapies
- Competitive scheduled hours with a focus on first shift work

What to Expect (Job Responsibilities):
- Perform daily clinical research activities for the employer's Comprehensive Cancer Center
- Coordinate correlative specimen study start-up and review clinical trial protocols for feasibility and accuracy
- Communicate with the Clinical Trials Office on protocol implementation and revisions
- Create study-specific educational materials for clinical research staff
- Ensure timely completion of tasks to facilitate study openings and review amendments to existing protocols

What is Required (Qualifications):
- Bachelor’s degree in biological sciences, health sciences, or a related field, or an equivalent combination of education and experience
- Minimum of one year of experience in a clinical research capacity
- Knowledge of medical terminology
- Proficiency in using Microsoft Software applications
- Strong computer skills

How to Stand Out (Preferred Qualifications):
- Experience in creating educational materials or conducting in-services for clinical research staff
- Familiarity with cancer research protocols and clinical trial processes

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