Employer Industry: Oncology Healthcare Services

Why Consider This Job Opportunity

• Competitive benefits package including Medical, Dental, Vision, Life Insurance, Short-term and Long-term disability coverage
• Generous PTO program and a 401k plan with company match
• Wellness program that rewards healthy lifestyle practices
• Tuition reimbursement and employee assistance program
• Opportunity to work at the largest community oncology provider in the country
  
  

What To Expect (Job Responsibilities)

• Coordinate critical document collection to facilitate timely opening of clinical trials
• Communicate and collaborate with central operations to identify and resolve regulatory issues
• Maintain protocol regulatory documents in compliance with local standard operating procedures
• Assist in the preparation of informed consent documents and regulatory packets for sponsor and IRB submissions
• Facilitate collection of site training documents and coordinate feasibility surveys with appropriate staff
  
  

What Is Required (Qualifications)

• High school diploma or equivalent required; some college coursework or relevant background preferred
• Minimum of three (3) years of experience in clinical research, regulatory affairs, or an oncology-related field required
• Proficiency in Microsoft Office
• Excellent communication skills and strong ability to multi-task
• Exceptional time management skills
  
  

How To Stand Out (Preferred Qualifications)

• Experience working with Sponsor Monitor representatives
  
  

#Oncology #ClinicalResearch #RegulatoryAffairs #CareerOpportunity #HealthcareJobs

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