Clinical Research Project Manager - Respiratory

Cleveland Clinic Health System

Cleveland, OH, US
Onsite
Phase i to iv clinical trial management
Fda regulations and gcp guidelines knowledge
Protocol development and regulatory document review
Cleveland Clinic Health System is seeking a Clinical Research Project Manager specializing in Respiratory Medicine to oversee administrative functions related to clinical trials. The ideal candidate should have relevant educational qualifications and clinical research experience, along with strong organizational and communication skills

Job Summary

  • This role involves overseeing the administrative functions of single and multi-institutional research trials within the Pulmonary Medicine department.
  • The successful candidate will facilitate key communications for academic coordination and provide clinical insight to support the design and conduct of clinical studies.
  • Cleveland Clinic offers a rewarding career with one of the most respected healthcare organizations in the world, emphasizing excellence and patient care.

Matching Summary

Match Score: 85

Cleveland Clinic Health System is seeking a Clinical Research Project Manager specializing in Respiratory Medicine to oversee administrative functions related to clinical trials. The ideal candidate should have relevant educational qualifications and clinical research experience, along with strong organizational and communication skills.

Skills & Requirements

Must-have

  • Phase I to IV clinical trial management
  • FDA regulations and GCP guidelines knowledge
  • Protocol development and regulatory document review
  • Site performance assessment and selection
  • Cross-functional team coordination

Nice-to-have

  • Strong communication skills for academic coordination
  • Experience with marketing strategies for recruitment
  • Ability to work in a fast-paced environment
  • Proactive approach to quality improvement initiatives

Key Requirements

  • Bachelor's Degree in Nursing, Science, Healthcare or Computer Science
  • Three years of clinical research experience as Study Coordinator or Project Manager
  • Completion of Human Subjects Research (HSR) training within 90 days
  • Knowledge of Code of Federal Regulations, ICH and GCP guidelines

Work Rights

Not specified

Tailored Resume

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