Senior Oncology Trials Operations Lead

University of North Carolina - Chapel Hill

Lowell (MA)

On-site

USD 90,000 - 130,000

Full time

14 days+
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Job summary

University of North Carolina at Chapel Hill is seeking a Clinical Operations Manager to oversee a large clinical research staff and ensure safe, compliant execution of oncology trials. You will report to the Assistant Director of Clinical Research Operations and coordinate resource allocation, data integrity, and SOP development.

Ideal candidates have advanced ICH GCP knowledge, extensive clinical research experience, and strong leadership abilities.

Qualifications

  • Advanced knowledge of ICH GCP, Federal Regulations and Guidelines; following regulations, procedures and protocols.
  • Clinical research experience.
  • Experience in interviewing/hiring and performance management.
  • Strong decision‑making and problem-solving skills.
  • Excellent organizational skills with ability to manage large volumes of information.
  • High level of accuracy and attention to detail.
  • Comfort with technology and strong computer skills.
  • Ability to plan work and coordinate multiple projects.

Responsibilities

  • Oversee and manage clinical research staff across disease teams.
  • Ensure safe, compliant, efficient conduct of oncology trials.
  • Allocate resources and oversee research compliance and data integrity.
  • Contribute to strategic planning, training, and SOP development.

Skills

ICH GCP
Clinical research
Hiring/Performance management
Decision making
Organization
Attention to detail
Tech savviness
Data documentation
Project coordination
Reports & SOPs
Interpersonal skills
Communication

Education

Master's degree in related field
Bachelor's degree + 2 years experience

Tools

Microsoft Office
EHR systems

Job description

University of North Carolina at Chapel Hill is seeking a Clinical Operations Manager to oversee a large clinical research staff and ensure safe, compliant execution of oncology trials. You will report to the Assistant Director of Clinical Research Operations and coordinate resource allocation, data integrity, and SOP development.

Ideal candidates have advanced ICH GCP knowledge, extensive clinical research experience, and strong leadership abilities.

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