Global Study Coordinator Translational Science Hub - VIE contract

at  Sanofi US

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.

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.

• 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.