Clinical Research Coordinator, Cardiovascular Device Clinical Trials

Responsibilities

• Oversight of all research-related activities
• Screens and evaluates prospective trial patients
• Follows up with enrolled trial patients
• Corresponds and coordinates with the Institutional Review Board and trial sponsors
• Facilitates and develops relationships with Sponsors for clinical trials
• Manages and tracks compliance with Federal and institution guidelines
• Educates patients on clinical trials and obtains informed consent
• Implements new trials, collaborates with multiple MD Principal Investigators, negotiates and maintains budgets, manages audits, and ensures adherence to study protocols
• Ensures implementation of mandated visits, medicine management, and symptom tracking

Requirements

• Bachelor's Degree or equivalent experience in Healthcare administration, Healthcare, Science or related field
• Three to five years of experience working directly in clinical trials involving human subjects
• Attention to detail and strong organizational skills
• US Driver’s license required

Qualifications

• Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Associate (CCRA) preferred
• Certification within 6 months of hire if less than 2 years full-time clinical research experience
• Must be fully vaccinated against seasonal Influenza and the COVID-19 virus or be exempt due to medical or personal reasons

Pay

Pay range: USD $57,553.60 - USD $96,761.60 /Yr.