Cardiac Trials Specialist - Clinical Research Coordinator

Sentara Health

Norfolk (VA)

On-site

USD 70,000 - 101,000

Full time

7 days ago
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Benefits offered by this job

Medical, Dental, Vision plans
Adoption, Fertility and Surrogacy Reim
Paid Time Off and Sick Leave
Paid Parental & Family Caregiver Leave
Emergency Backup Care
Long-Term Disability
Short-Term Disability
Critical Illness plans
Life Insurance
401k/403B with Employer Match
Tuition Assistance
Student Debt Pay Down
Pet Insurance
Legal Resources Plan
Annual discretionary bonus

Job summary

Sentara Heart Hospital, located on the campus of Sentara Norfolk General Hospital in Norfolk, VA, is seeking a Clinical Research Coordinator to manage and coordinate all aspects of conducting clinical trials.

The successful candidate will apply protocol requirements, ensure compliance with GCP, recruit and enroll subjects, maintain regulatory documents, and serve as a liaison among investigators, the IRB, and the sponsor.

Qualifications

  • Bachelor's degree required.
  • BLS certification required within 90 days of hire.
  • CCRPs/ACRP certifications required within 3 years of employment.
  • Minimum 3 years of clinical research or clinical experience.

Responsibilities

  • Coordinate all aspects of conducting clinical trials within Sentara Healthcare.
  • Ensure studies are conducted in conformance with protocol guidelines and GCP.
  • Recruit, screen, enroll and follow up with eligible subjects per protocol.
  • Maintain accurate and complete regulatory documentation.
  • Act as liaison between investigators, the IRB and the sponsor.

Education

Bachelor's degree

Job description

Sentara Heart Hospital, located on the campus of Sentara Norfolk General Hospital in Norfolk, VA, is seeking a Clinical Research Coordinator to manage and coordinate all aspects of conducting clinical trials.

The successful candidate will apply protocol requirements, ensure compliance with GCP, recruit and enroll subjects, maintain regulatory documents, and serve as a liaison among investigators, the IRB, and the sponsor.

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