Lead Clinical Scientist – End-to-End Studies (Hybrid)

CSL

Thatcham

Hybrid

GBP 90,000 - 130,000

Full time

9 days ago
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Job summary

CSL Seqirus is seeking a Principal Clinical Scientist hybrid role, based in Maidenhead, with global collaboration across US and Australia. You will lead studies end-to-end—from protocol development, start-up, execution, data interpretation, to close-out with the clinical study report.

Strong CRO partnership and regulatory submission experience are preferred. This role emphasizes scientific leadership within a full-outsource operating model, not routine in-house trial activity, and offers

Qualifications

  • Hands-on experience with clinical studies from protocol development to close-out
  • Experience writing clinical study protocols and clinical study reports
  • Experience working in a full-outsource/CRO-dependent operating model

Responsibilities

  • Lead all scientific elements of clinical studies from protocol development through study execution to a final clinical study report
  • Write and/or take responsibility for study protocols, clinical study reports and other critical study documents
  • Manage day-to-day relationships with CROs under a full-outsource operating model
  • Collaborate with cross-functional study teams
  • Contribute to the scientific interpretation of clinical data and supporting documentation
  • Build relationships across the wider team including US and Australia

Skills

Clinical studies
Protocol development
Study execution
Clinical study reports
CRO management
Cross-functional collaboration

Job description

CSL Seqirus is seeking a Principal Clinical Scientist hybrid role, based in Maidenhead, with global collaboration across US and Australia. You will lead studies end-to-end—from protocol development, start-up, execution, data interpretation, to close-out with the clinical study report.

Strong CRO partnership and regulatory submission experience are preferred. This role emphasizes scientific leadership within a full-outsource operating model, not routine in-house trial activity, and offers

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