Clinical Research Program Coordinator - Ri Gene Therapy

stantonlab.info

Main Campus, OH, United States
On-site
Manage research portfolio
Grant budgets and irb protocols
Coordinate subcontracts
The Clinical Research Program Coordinator position at Stanton Lab involves managing and coordinating research projects, ensuring compliance with IRB protocols, and overseeing funding and data management across multiple sites. The role requires strong organizational and communication skills, as well as a background in clinical research or project management

Job Summary

  • Coordinates and manages the department/center’s research portfolio, maintaining working knowledge of projects in process and funded projects including grant budgets and IRB protocols.
  • Responsible for administrative management, organization of, and participation in program meetings and teleconferences, including scientific meetings with corporate and non-profit partners.
  • Manages and oversees IRB process for program projects and associated sites, ensuring sites are submitting accurate and timely IRB submissions, and maintain associated regulatory documents.

Matching Summary

Match Score: 85

The Clinical Research Program Coordinator position at Stanton Lab involves managing and coordinating research projects, ensuring compliance with IRB protocols, and overseeing funding and data management across multiple sites. The role requires strong organizational and communication skills, as well as a background in clinical research or project management.

Skills & Requirements

Must-have

  • Manage research portfolio
  • Grant budgets and IRB protocols
  • Coordinate subcontracts
  • Develop and implement processes
  • Manage program and project funds
  • Track projects and initiatives

Nice-to-have

  • Demonstrated leadership skills
  • Self-directed, results driven
  • Ability to work independently and as part of a team

Key Requirements

  • Bachelor’s degree preferred or Associate degree with two years clinical research experience or project management experience
  • ACRP or SOCRA certification, preferred
  • Two years clinical research experience or project management experience

Work Rights

Not specified

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