Clinical Research Specialist II- FT Orthopedic Services

University Hospitals   Cleveland Heights, OH   Full-time
This job is no longer available.
Job Posting Shared.
Job Posting Reminder Sent.

Position Overview/Duties:

Works with the Principal Investigator to coordinate all aspects of implementation of assigned multiple and or complex clinical research trials.

  • Responsible for submission of related documents to the appropriate regulatory review committees and maintenance of regulatory files.
  • Performs all activities related to clinical research studies including but not limited to, screening participants for eligibility and recruitment, obtains informed consent, educates participants regarding study requirements and completes case report forms, CRF.
  • Responsible for in depth knowledge of protocol requirements and Good Clinical Practice guidelines.
  • Documents, records and assimilates accurate participant records and study records to ensure documentation compliance with sponsor guidelines, standard operating procedures and internal and external regulatory agencies.
  • Establish and maintain communications with Investigator, Sponsor and internal constituents.
  • Mentorship of the clinical research process to the junior clinical research staff.
  • Performs other related duties as assigned or required. 

Position Overview/Duties:

Works with the Principal Investigator to coordinate all aspects of implementation of assigned multiple and or complex clinical research trials.

  • Responsible for submission of related documents to the appropriate regulatory review committees and maintenance of regulatory files.
  • Performs all activities related to clinical research studies including but not limited to, screening participants for eligibility and recruitment, obtains informed consent, educates participants regarding study requirements and completes case report forms, CRF.
  • Responsible for in depth knowledge of protocol requirements and Good Clinical Practice guidelines.
  • Documents, records and assimilates accurate participant records and study records to ensure documentation compliance with sponsor guidelines, standard operating procedures and internal and external regulatory agencies.
  • Establish and maintain communications with Investigator, Sponsor and internal constituents.
  • Mentorship of the clinical research process to the junior clinical research staff.
  • Performs other related duties as assigned or required. 

Qualifications:

  • Bachelor Degree required and 3 + years of research experience
  • Certification in Human Subjects Protection and CTSC cultural competency training, must be obtained within 3 months of hire.
  • Research certification preferred e.g., SOCRA or ACRP.

This job is no longer available.

University Hospitals

Cleveland Heights, OH