Employer Industry: Healthcare Research

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Work remotely from anywhere in the U.S., with limited in-office presence
- Engage in meaningful work that supports oncology clinical trials
- Collaborative and inclusive work environment that values diverse perspectives
- Minimal domestic travel required (1-2 field visits per month)

What to Expect (Job Responsibilities):
- Track trial progress across participating sites, including accrual and regulatory submissions
- Correspond with sites to support trial activities, addressing questions and providing updates
- Conduct onsite and remote monitoring visits, completing monitoring reports
- Verify documentation of consent and eligibility criteria for patient inclusion
- Gather and organize essential regulatory documents from participating sites

What is Required (Qualifications):
- Bachelor's degree required
- Minimum of 1-2 years of directly related work experience
- Ability to work independently with general supervision
- Excellent written and oral communication skills
- Strong organizational and time management skills, with attention to detail

How to Stand Out (Preferred Qualifications):
- Working knowledge of clinical research protocols
- Problem-solving skills, including the ability to gather information and develop alternatives
- Analytical skills to identify and resolve issues effectively

#HealthcareResearch #ClinicalTrials #RemoteWork #CareerOpportunity #DiversityInclusion

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