Employer Industry: Medical Device and Clinical Research

Why Consider This Job Opportunity

• Salary up to $186,700 plus bonus eligible and benefits
• Opportunity for career advancement and growth within the organization
• Work remotely anywhere within the United States, with a preference for Eastern time zone
• Supportive and collaborative work environment
• Chance to make a positive impact on patient outcomes in the field of stroke therapies
  
  

What To Expect (Job Responsibilities)

• Provide high-quality site monitoring and management for the Study Operations team within Clinical Shared Services
• Proactively communicate with investigators, colleagues, and vendors to ensure clinical quality and compliance
• Conduct clinical research activities in accordance with applicable regulations and guidelines
• Manage overall clinical site activities and provide oversight to Clinical Research Associates (CRAs)
• Develop and implement enrollment and recruitment strategies for clinical studies
  
  

What Is Required (Qualifications)

• Bachelor’s Degree in a health/science field (RN, BSN, MBBS, DPharm)
• 4 years of industry experience in a clinical study operations role within Medical Device or Pharma
• 3 years of independent site management responsibilities and data monitoring experience
• Demonstrated independence in conducting Site Qualification and Site Initiation Visits
• Working knowledge of GCP/ICH guidelines and federal/local regulations
  
  

How To Stand Out (Preferred Qualifications)

• Master's, MBA, or PhD
• Experience performing Site Close-Out Visits
• ACRP CCRA Certification or SOCRA CCRP Category 3 Certification
• Medical Device monitoring experience
• Global clinical trial experience and EUMDR working knowledge
  
  

#MedicalDevices #ClinicalResearch #RemoteWork #CareerOpportunity #CompetitivePay

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