Employer Industry: Oncology Healthcare

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Supportive and collaborative work environment
- Chance to make a positive impact in cancer research and patient care
- Work remotely with a flexible schedule
- Engage in innovative practices within the largest community oncology provider in the country

What to Expect (Job Responsibilities):
- Manage regulatory processes and procedures for clinical trials
- Prepare protocol documents that comply with regulatory and institutional requirements
- Assist with critical document collection and maintenance for timely trial openings
- Communicate with central operations to resolve regulatory issues
- Monitor and report serious adverse events (SAEs) to sponsors and Institutional Review Boards (IRBs)

What is Required (Qualifications):
- High School Diploma required; Associate's degree in a clinical or scientific-related discipline preferred
- Minimum of three (3) years of experience in clinical research, regulatory affairs, or an oncology-related field
- Proficiency in Microsoft Office
- Strong communication skills and ability to multi-task
- Excellent time management skills

How to Stand Out (Preferred Qualifications):
- Experience working with Sponsor Monitor representatives
- Experience in oncology-related fields is a plus
- Familiarity with regulatory documents and submission processes
- Background in quality assurance initiatives within clinical trials

#OncologyHealthcare #RemoteWork #ClinicalResearch #CareerGrowth #PatientCare

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