Associate Director, Global Clinical Project Leadership (Hybrid)

CTI Clinical Trial and Consulting Services

Covington (KY)

On-site

USD 120,000 - 180,000

Full time

4 days ago
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Benefits offered by this job

Hybrid work from home opportunities

Job summary

CTI Clinical Trial and Consulting Services is seeking an Associate Director to lead the management of Phase I–IV trials across geographic and functional areas, ensuring projects are delivered on time, on budget and with quality. You will mentor staff and advance trial processes to improve execution and organizational capability.

You will work with Clinical Project Managers and CPCs, ensure compliance with ICH/GCP and regulatory guidelines, act as the senior sponsor interface, and help resolve

Qualifications

  • Bachelor’s degree in allied health fields with clinical trial management experience or equivalent.
  • At least 10 years of clinical research experience and/or clinical project management.
  • Experience in management of clinical trials.

Responsibilities

  • Plan, implement, facilitate and evaluate full execution of assigned clinical trials.
  • Ensure compliance with ICH/GCP and regulatory guidelines.
  • Coordinate CPMS/CPCs and liaise with clients and executives.
  • Manage budgets and timelines; escalate issues and implement solutions.
  • Provide leadership in process improvement and staff development.
  • Mentor CPMs and CPC staff to enhance skills.

Skills

Clinical project management
Global trial management
Staff mentoring

Education

Bachelor’s degree in allied health fields such as nursing, pharmacy or health science

Job description

CTI Clinical Trial and Consulting Services is seeking an Associate Director to lead the management of Phase I–IV trials across geographic and functional areas, ensuring projects are delivered on time, on budget and with quality. You will mentor staff and advance trial processes to improve execution and organizational capability.

You will work with Clinical Project Managers and CPCs, ensure compliance with ICH/GCP and regulatory guidelines, act as the senior sponsor interface, and help resolve

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