Global Study Manager, Translational Science Hub

The Translational Science Hub will link world-class researchers in Queensland with Sanofi scientists located in France and the US. This will create a unique global vaccines R&D network focused on mRNA technology and Translational Science.    

This is a first-of-its-kind partnership with the Queensland Government, University of Queensland and Griffith University and will place Australia at the forefront of global vaccine development and biomedical research.   

We are an innovative global healthcare company, driven by one purpose: We chase the miracles of science to improve people’s lives. Our team, across some 100 countries, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the centre of our ambitions.

About the Role   

This 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 individual will be accountable for delivering studies within the expected timelines, budget and quality. The role will work closely with the Director of Clinical Operations to build and establish clinical trial operations for the TSH, bringing synergies to the studies and proposes innovation in the operationalization of studies.  

Responsibilities  

• Work with the clinical team to ensure operational aspects of the study are considered in ensuring an efficient study design   
• Coordinate the Clinical Team with the Clinical Sciences representative (Clinical Team is composed of representatives from Global Clinical Department platforms, GCI, GPV, RA, Clinical Supply Chain, and other relevant departments) for the operational aspect of the study.  Ensure study feasibility is properly done and considered working with other functions and integrate feedback in study plan and risks (RA timelines, country selection, recruitment potentials, budget needs).  
• Develop and maintain optimized study planning with other functions  
• Provide assumptions for number of sites and enrollment rates for budget and planning purposes for all studies within a program  
• Integrate and follow up study risks, ensuring alignment of all Clinical team members and functions
• Work with CROs for the operational delivery of the studies  
• Develop clinical trial networks for the program through the TSH 

To be successful in this role, we believe you should have the following;  

• Bachelors degree in relevant scientific field or equivalent qualification  
• 6+ years experience in vaccine or clinical research is preferred  
• Clinical Trial experience required  
• Formal training in GCP methods  
• Proven track record in delivery high quality GCP-compliant Clinical Trials
• Project management and budget management experience  
• Experience in working with CROs in delivery of clinical trials  
• Demonstrated advanced team and negotiation skills  
• Work experience in a global environment with multicultural teams 

Interested? Please reach out to Stuart Gates from our Talent Acquisition team to express your interest!  

This is a rare opportunity that doesn’t come up often, so apply online today and don’t miss out.   

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

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