Global Study Manager - TSH

Sanofi

Brisbane

On-site

AUD 180,000 - 250,000

Full time

12 days ago

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Job summary

Sanofi is seeking a Global Study Manager – TSH in Woolloongabba, Australia. The role leads operational delivery of studies, partnering with Clinical Operations, GCI, GPV, and CROs to ensure on-time, on-budget delivery with high quality.

You will contribute to feasibility assessments, risk logs, and budget planning while developing clinical trial networks and vendor partnerships for global programs.

Qualifications

  • 6+ years of experience in clinical research, preferably in vaccines.
  • Proven track record of delivering high-quality, GCP-compliant clinical trials.
  • Project management and budget management experience.

Responsibilities

  • Study design input: build operationally feasible study designs.
  • Cross-functional coordination with Global Clinical Department platforms, GCI, GPV, RA, Clinical Supply Chain and others.
  • Feasibility and risk management with input from RA timelines, country selection, recruitment potential, budget needs.
  • Plan and budget assumptions for optimized study plans and enrollment rates.
  • Vendor and CRO management for operational delivery of studies.
  • Network and partnership development for the program through the Translational Science Hub (TSH).

Skills

Clinical research
Vaccine trials
Project management
Budget management

Education

Bachelor's degree in a relevant scientific field
Formal training in GCP

Job description

Job Title: Global Study Manager – TSH
Location: Woolloongabba, AUS
Job Type: Permanent, Full Time
About the Job:
  • The Global Study Manager is a key role within the Clinical Team, responsible for the operational delivery of all studies within a specific project of the Translational Science Hub (TSH). The role is accountable for delivering studies on time, within budget and to the required quality standards. Working closely with the Head of Clinical Operations, the Global Study Manager creates synergies across studies and proposes innovative approaches to study operationalization.
Key Responsibilities:
  • Study design input: Work with the Clinical Team to ensure operational considerations are built into an efficient study design.
  • Cross-functional coordination: Coordinate the Clinical Team with representatives from Global Clinical Department platforms, GCI, GPV, RA, Clinical Supply Chain and other relevant departments on all operational aspects of the study.
  • Feasibility and risk management: Ensure study feasibility assessments are completed with input from other functions (RA timelines, country selection, recruitment potential, budget needs). Integrate the findings into the study plan and risk log and follow up on risks to keep all Clinical Team members and functions aligned.
  • Planning and budget assumptions: Develop and maintain optimized study plans with other functions. Provide assumptions on the number of sites and enrollment rates for budget and planning purposes across all studies in the program.
  • Vendor and CRO management: Work with CROs on the operational delivery of studies.
  • Network and partnership development: Develop clinical trial networks and vendor partnerships for the program through the TSH.
Interactions
  • Internal: Members of the Clinical Team, including the Global Clinical Development Strategic Expert and the Global Biostatistician. The role works closely with the Head of Clinical Operations to build the TSH's clinical trial capacity.
  • External: Clinical Research Organizations, external partners, sites and investigators.
Requirements
Qualifications:
  • Bachelor's degree in a relevant scientific field, or equivalent qualification
  • Formal training in GCP
Experience
  • 6+ years of experience in clinical research, preferably in vaccines
  • Clinical trial experience (required), including experience in vaccine trials
  • Proven track record of delivering high-quality, GCP-compliant clinical trials
  • Project management and budget management experience
Desirable
  • Experience working with CROs on full-service clinical trials
  • Advanced team-working and negotiation skills
  • Experience working in a global environment with multicultural teams
Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

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