Added
9 minutes ago
Type
Full time
Salary
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Related skills

gcp clinical operations ich regulatory submissions irb

๐Ÿ“‹ Description

  • Provide leadership to the Site Start-up (SSU) department and guide strategy for SSU growth, people
  • Collaborate with Regulatory, Sites, IRB/EC, CA and Contracts to ensure SSU delivery and client
  • Develop SSU framework, tools and methodologies with the Head of Site Start Up to enable project
  • Oversee SSU programs, including large or complex programs, across global and regional contexts.
  • Support cross-functional planning and governance with Clinical Operations, Project Management and
  • Drive process optimization to improve SSU profitability and meet budget targets.

๐ŸŽฏ Requirements

  • Bachelors in life sciences or related field; 12+ years in clinical research with extensive SSU
  • Experience in CRO environments and people management.
  • Expert knowledge of GCP/ICH guidelines and the clinical development process.
  • Proven leadership, team management and cross-functional collaboration skills.
  • Experience with MS Office; familiarity with clinical software (CTMS, eTMF, EDC).
  • Excellent communication, organization, and stakeholder management abilities; English fluency.

๐ŸŽ Benefits

  • Discretionary annual bonus, private medical insurance, MultiSport Card, life insurance, pension
  • Remote-friendly role with potential for UK/EU-based work locations.
  • Career development, growth opportunities and supportive SSU leadership.
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