(global) Study Manager - Fsp

Thermo Fisher Scientific UK

Fully client-embedded (onsite)
Global clinical study management experience
End-to-end study delivery from feasibility to csr
Ph ii and ph iii trial experience
Thermo Fisher Scientific UK is seeking a Global Study Manager to oversee clinical operations for a leading bio-pharma client. The role involves comprehensive management of clinical studies, ensuring adherence to timelines, budgets, and quality standards while effectively communicating with stakeholders

Job Summary

  • This fully client-embedded role is accountable for delivering clinical operation activities of the study until archiving with a focus on upper quartile performance.
  • The Global Study Manager must lead empowered matrix teams to achieve operational deliverables including study initiation, recruitment tracking, and safety management plans.
  • Candidates must demonstrate proven end-to-end global experience across NA, EMEA, APAC, and LATAM regions with strong vendor oversight capabilities.

Matching Summary

Match Score: 85

Thermo Fisher Scientific UK is seeking a Global Study Manager to oversee clinical operations for a leading bio-pharma client. The role involves comprehensive management of clinical studies, ensuring adherence to timelines, budgets, and quality standards while effectively communicating with stakeholders.

Skills & Requirements

Must-have

  • Global clinical study management experience
  • End-to-end study delivery from feasibility to CSR
  • Ph II and Ph III trial experience
  • Cross-functional team leadership
  • Vendor and CRO management
  • Clinical budget management
  • Risk mitigation and quality compliance

Nice-to-have

  • Experience with China, Japan, Africa markets
  • Pivotal study registration exposure
  • Competent authority inspection involvement
  • Protocol and ICF development input
  • Strong negotiation skills for complex topics

Key Requirements

  • Bachelor's degree in life sciences or related discipline
  • At least 5+ years of relevant global study management experience
  • Proven experience from study feasibility to Clinical Study Report (CSR)
  • Must have at least Phase II and Phase III experience

Work Rights

Not specified

Tailored Resume

Cover Letter