Clinical Studies Coordinator Ii, Cardiology Research

Wake Forest University Health Sciences

Unknown, Unknown, US
Base: $26.55 - $39.85; bonus/equity: not specified...
Onsite
Coordinates research studies
Recordkeeping systems and procedures
Compilation, registration and submission of data
Wake Forest University Health Sciences is seeking a Clinical Studies Coordinator II for cardiology research. The role involves coordinating complex research studies, managing compliance, and assisting with patient recruitment, requiring a bachelor's degree and two years of clinical research experience

Job Summary

  • Under departmental direction, coordinates activities to support multiple research studies of all phases.
  • Plays an active role in recruitment of patients to study and obtains or assists the Principal Investigator in obtaining informed consent from subjects.
  • Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more.

Matching Summary

Match Score: 85

Wake Forest University Health Sciences is seeking a Clinical Studies Coordinator II for cardiology research. The role involves coordinating complex research studies, managing compliance, and assisting with patient recruitment, requiring a bachelor's degree and two years of clinical research experience.

Salary

Base: $26.55 - $39.85; Bonus/Equity: Not specified; Benefits: Yes

Skills & Requirements

Must-have

  • coordinates research studies
  • recordkeeping systems and procedures
  • compilation, registration and submission of data
  • recruitment of patients to study
  • abstracts data from medical record
  • completes case report forms
  • maintains source documents

Nice-to-have

  • excellent interpersonal skills
  • strong organizational skills
  • sensitivity to intercultural relations
  • high level of integrity and honesty

Key Requirements

  • Bachelor's degree with two years experience
  • SOCRA or ACRP Certification preferred
  • CITI certification for Human Subject Research
  • EPIC/WakeOne proficiency
  • OnCore/WISER Clinical Trial Management System proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter