Employer Industry: Oncology Research and Healthcare

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Work remotely from the comfort of your home
- Contribute to high-quality, evidence-based cancer care that impacts patients' lives
- Collaborative work environment with a focus on quality improvement measures
- Engaging responsibilities in regulatory affairs and clinical trial management

What to Expect (Job Responsibilities):
- Assist with critical document collection and maintenance to ensure 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
- Support local QA initiatives and lead quality improvement measures to assist investigators
- Prepare informed consent documents and regulatory packets for sponsor and IRB submissions

What is Required (Qualifications):
- High School Diploma required
- Minimum of one (1) year of experience in clinical research, regulatory affairs, and/or an oncology-related field required
- Experience in Microsoft Office
- Strong communication skills and the ability to multi-task effectively
- Excellent 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
- Additional experience in clinical research, regulatory affairs, and/or an oncology-related field is preferred

#OncologyResearch #ClinicalTrials #RemoteWork #HealthcareCareers #RegulatoryAffairs

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