Clinical Research Project Manager - Respiratory

Cleveland Clinic Health System

Cleveland, Ohio, United States
Not specified; not specified; not specified
**
Phase i to iv clinical trial management
Fda regulations and gcp guidelines knowledge
Irb and protocol document coordination
** Cleveland Clinic Health System is seeking a Clinical Research Project Manager for its Respiratory department at the Main Campus in Cleveland, Ohio. The role involves overseeing clinical trials, managing research coordinators, and ensuring compliance with regulatory standards. **

Job Summary

  • Join Cleveland Clinic's Main Campus to oversee the administrative functions of the Integrated Hospital Care Institute research portfolio specifically in Pulmonary Medicine.
  • The role involves managing daily operations for Phase I to IV clinical trials while facilitating key communications for academic coordination and providing clinical insight.
  • Candidates must maintain professional relationships with sponsors and interact with Finance and Legal Departments to facilitate budget and contract execution.

Matching Summary

Match Score: 75

** Cleveland Clinic Health System is seeking a Clinical Research Project Manager for its Respiratory department at the Main Campus in Cleveland, Ohio. The role involves overseeing clinical trials, managing research coordinators, and ensuring compliance with regulatory standards. **

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • Phase I to IV clinical trial management
  • FDA regulations and GCP guidelines knowledge
  • IRB and protocol document coordination
  • Clinical research team leadership
  • Site performance assessment and management

Nice-to-have

  • Society of Clinical Research Associates certification
  • Association of Clinical Research Professionals certification
  • Supervisory experience with research staff
  • Strong communication skills for academic coordination

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 training within 90 days
  • Knowledge of Code of Federal Regulations and ICH guidelines

Work Rights

Not specified

Tailored Resume

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