Global Study Coordinator Translational Science Hub - VIE contract

Global Study Coordinator Translational Science Hub - VIE Contract

• Location: Australia, Woolloongabba
• Target start date: 01/12/2024

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address. 
About the job

Looking to launch your career at the cutting edge of healthcare? Join Sanofi for a chance to develop with mentoring and guidance from inspirational leaders while helping to make an impact on the lives of countless people worldwide. As Global Study Coordinator Translational Science Hub VIE in our Clinical Operations team you will work closely with the members of the clinical team including the Global Clinical Development Strategic Expert and Global Biostatistician. The role will interface directly with Clinical Research Organizations, external partners, sites and investigators and will work closely with the Director of Clinical Operations to build the clinical trial capacity of the Translational Science Hub (TSH). This is a key role within the Clinical Team responsible for the operational delivery of all studies within a specific project of the TSH. You will be accountable for delivering studies within the expected timelines, budget and quality.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

Main responsibilities:

• Work with the clinical team to ensure operational aspects of the study are considered in ensuring an efficient study design.
• Coordinates the Clinical Team with the Clinical Sciences representative (Clinical Team is composed of representatives from Global Clinical Department platforms, Global Clinical Immunology - GCI, Global Pharmacovigilance - GPV, Regulatory Affairs - RA, Clinical Supply Chain, and other relevant departments) for the operational aspects of the study. Ensures study feasibility is properly done and considered working with other functions and integrates feedback in study plan and risks (RA timelines, country selection, recruitment potentials, budget needs).
• Be accountable to develop and maintain optimized study planning with other functions.
• Be responsible for providing assumptions for number of sites and enrollment rates for budget and planning purposes for all studies within a program.
• Integrates and follows up study risks, ensuring alignment of all Clinical team members and functions.
• Work with Contract Research Organization - CROs for the operational delivery of the studies.
• Develop clinical trial networks for the program through the TSH.

About you

Experience:

• 1-2 years of experience in vaccine or clinical research is preferred.

Soft and Technical skills:

• Clinical Trial experience required.
• Formal training in Good Clinical Practice - 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 is desirable.
• Demonstrated advanced team and negotiation skills is desirable.
• Work experience in a global environment with multicultural teams is desirable.

Education:

• Master's degree in relevant scientific field or equivalent qualification.

Languages:

• Fluent French & English.

Why choose us?

iMove is a unique program tailored for European youth interested in challenging themselves with meaningful assignments across the globe. At Sanofi we have a strong ambition to invest in young talents who will drive the success of Sanofi tomorrow.

Sanofi’s Work Abroad Program, iMove, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our iMove Work Abroad Program is a unique opportunity to make a difference through your work.

#LI-EUR

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.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!