Clinical Research Coordinator II

7 days ago

Cleveland, Ohio, United States MetroHealth Full time
Job Summary

We are seeking a highly motivated and organized Clinical Research Coordinator II to join our team at MetroHealth. The successful candidate will be responsible for planning, delivering, documenting, and observing the progress of subjects enrolled in research studies in accordance with study protocols.

Key Responsibilities
  • Assist and collaborate with Research department leadership in the development of study budgets that are representative of the procedures outlined within protocols.
  • Uphold the mission, vision, values, and customer service standards of The MetroHealth System.
  • Work with an Institutional Review Board (IRB) to ensure compliance with regulations and guidelines.
  • Develop and maintain accurate and detailed records of research studies, including subject enrollment, data collection, and study progress.
  • Communicate effectively with research team members, study participants, and other stakeholders to ensure smooth study execution.
Requirements
  • Associate Degree in a Science, Healthcare, or other related field.
  • Three years of experience working as a clinical research coordinator working with human subjects, or two years of experience and one of the following certifications:
  • Certified Clinical Research Coordinator (CCRC) by the Association of Clinical Research Professionals (ACRP)
  • Certified Clinical Research Professional by the Society of Clinical Research Associates (SOCRA)
  • Advanced Clinical Research Coordinator Certification (ACRCC) by the Certified Clinical Research Professional Society (CCRPS)
  • In lieu of degree, five years of experience as a clinical research coordinator working with human subjects.
  • Experience working with an Institutional Review Board (IRB).
  • Good organizational and problem-solving skills.
  • Proficiency in personal computers and various software/database applications (i.e. EPIC, OnBase, and the Microsoft Office Suite).
  • Excellent interpersonal, written, and verbal communication skills.
  • Maintains competencies in clinical areas.
  • Willing and able to adhere to flex work schedules as needed, including weekend hours.
  • Ability to interact effectively with a wide range of cultural, ethnic, racial, and socioeconomic backgrounds.
Preferred Qualifications
  • Bachelor's Degree in Science or another related field.
  • Experience with finance/billing.
  • Currently a Certified Clinical Research Coordinator (CCRC) by the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA).
Physical Requirements
  • May sit, stand, stoop, bend, and ambulate intermittently during the day.
  • May need to sit or stand for extended periods.
  • See in the normal visual range with or without correction.
  • Hear in the normal audio range with or without correction.
  • Finger dexterity to operate office equipment required.
  • May need to lift up to twenty-five (25) pounds on occasion.
  • Ability to communicate in face-to-face, phone, email, and other communications.
  • Ability to see computer monitor and departmental documents.
  • Requires some exposure to communicable diseases or body fluids.
  • Requires some exposure to chemicals and cleaning products.

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