Employer Industry: Healthcare Research

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Work remotely, with periodic presence required in Columbus, Ohio
- Engage in meaningful work that contributes to cancer research and patient care
- Collaborative environment with a multidisciplinary team
- Competitive standard working hours of 40 hours per week

What to Expect (Job Responsibilities):
- Coordinate and perform daily clinical research activities in accordance with the Total Cancer Care protocol
- Assess patient records to identify eligible participants for clinical research studies
- Collect, extract, and analyze clinical research data while ensuring data validity
- Support compliance with regulatory, Institutional Review Board (IRB), and study requirements
- Assist in coordinating specimen procurement and quality control processes

What is Required (Qualifications):
- Bachelor's degree in biological sciences, health sciences, or a related field, or equivalent combination of education and experience
- Minimum of one year of experience in a clinical research capacity
- Experience in data collection, data entry, and data reporting
- Proficiency in Microsoft software applications
- Knowledge of medical terminology, biospecimens, tissue procurement, and surgical pathology is desired

How to Stand Out (Preferred Qualifications):
- Familiarity with clinical research protocols and procedures
- Experience working with cancer-related research projects
- Strong analytical and problem-solving skills
- Excellent communication and teamwork abilities
- Previous experience in a regulatory compliance environment

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