Clinical Operations Manager Cluster South

Added
25 days ago
Type
Full time
Salary
Salary not provided

Related skills

gcp monitoring clinical research ich guidelines site management

πŸ“‹ Description

  • Accountable for site-related study execution activities for assigned studies, including startup
  • Oversee site evaluation/selection, contracts/budget negotiation, regulatory submissions
  • Ensure adherence to GCPs, ICH Guidelines, AbbVie SOPs, Monitoring Plans, and quality standards in
  • Ensure audit readiness; support pre-audit activities for GCP, and manage audits, CAPA, and
  • Manage resources for assigned team; allocate resources aligned with study timelines and AbbVie

🎯 Requirements

  • Bachelors or equivalent degree (health related preferred).
  • Minimum 3 years of monitoring experience.
  • Strong interpersonal, cross-functional collaboration, and mentoring skills.
  • Excellent planning/organizational abilities; experience across multiple therapeutic areas/phases.
  • Ability to make timely, high-quality decisions with data; independent and proactive ownership
  • Ability to work with risk/ambiguity and adapt quickly.

🎁 Benefits

  • AbbVie equal opportunity employer; inclusive culture and opportunities for development.
  • Global exposure through cross-functional collaboration and potential participation in task forces.
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