Employer Industry: Oncology Services

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Flexible remote work arrangement
- Supportive and collaborative work environment
- Chance to contribute to high-quality, evidence-based cancer care
- Engaging role with responsibilities in clinical trials and regulatory affairs

What to Expect (Job Responsibilities):
- Manage research regulatory and administrative activities of clinical trials for the practice
- Prepare protocol documents that comply with regulatory and institutional requirements
- Maintain Protocol Regulatory Documents in compliance with local Standard Operating Procedures
- Communicate and collaborate with central operations to identify and resolve regulatory issues
- Assist with preparation of Informed Consent Documents and regulatory packets for sponsor and IRB submissions

What is Required (Qualifications):
- High School Diploma required
- Minimum of three (3) years of experience in clinical research, regulatory affairs, and/or an oncology-related field required
- Experience in Microsoft Office
- Excellent communication skills and strong ability to multi-task
- Strong time management skills

How to Stand Out (Preferred Qualifications):
- Associate's degree in a clinical or scientific-related discipline preferred
- Experience working with Sponsor Monitor representatives preferred
- Background in clinical research, regulatory affairs, and/or oncology-related field preferred

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