Employer Industry: Oncology Services

Why consider this job opportunity:
- Opportunity for career advancement and growth within a leading community oncology provider
- Supportive work environment focused on delivering high-quality, evidence-based cancer care
- Involvement in significant clinical trials and research initiatives
- Contribute to the fight against cancer and make a meaningful impact in patients' lives
- Work in a remote capacity while collaborating with a dedicated team across multiple locations

What to Expect (Job Responsibilities):
- Assist with critical document collection and maintenance to facilitate timely trial openings and audit readiness
- Communicate and collaborate with central operations to identify and resolve regulatory issues
- Maintain protocol regulatory documents in compliance with local Standard Operating Procedures
- Assist with preparation of informed consent documents and regulatory packets for sponsor and IRB submissions
- Monitor and report serious adverse events (SAEs) to sponsors and IRBs

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
- Must possess excellent communication skills, strong multitasking abilities, and excellent time management skills
- Associate's degree in a clinical or scientific-related discipline preferred

How to Stand Out (Preferred Qualifications):
- Experience working with sponsor monitor representatives
- Experience in clinical research, regulatory affairs, and/or an oncology-related field is preferred

#OncologyCare #ClinicalResearch #RegulatoryAffairs #RemoteWork #CareerGrowth

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