Sanofi
Biopharma
JuniorClinicalscientist
“Junior Clinical scientist at Sanofi. Skills: Clinical research, Data management, Regulatory affairs. Prepare and review study documents. Support medical answers to Health Authorities”
What You'll Achieve.
Advance clinical research; Ensure scientific rigor; Ensure data quality; Ensure regulatory compliance; Support delivery of high-quality clinical trials; Bring innovative treatments to patients; Streamline processes; Accelerate the path from research to life-changing medicines; Improve the lives of millions of people globally; Make drug development quicker and more effective
Industry & Context.
Analytical mindset; Proactively identify risks; Problem solving
What They're Looking For.
Must Have
Bachelor's degree in a scientific discipline, 1 year of training/work experience, Leadership to give directions and organize the activities on behalf of the Clinical Research Director, Well organized with the ability to handle multiple tasks and prioritize, working autonomously and efficiently providing status reports, quality focused, able to develop good practices, using a critical data-driven and risk management approach, Ability to analyze and interpret data-driven decision dashboards, familiar with digital tools such as data analytics or agility to use them, Ability to synthesize the information, good presentation skills, able to anticipate and timely escalate issues, able to execute action plans, Team and results oriented, Great communication skills (verbal and written), experience of working internationally with English skills (verbal and written if English is not the native language)
Nice to Have
Ph. D. , Pharm. D. , M. D. , or similar advanced degree, scientific expertise or interest and ability to learn in the domain of assigned study/project
What You'll Do.
Prepare and review study documents
Support medical answers to Health Authorities
Contribute to risk management plan
Update study documents
Develop study specific training material
Participate to Investigator training
Contribute to centralized monitoring strategy
Support CRD for Clinical Case review
Support CRD in implementing Steering committees
How You'll Work.
Team & Collaboration
Coordinate key stakeholders; Work with international teams; Work with product team; Collaborate with investigators; Collaborate with Health Authorities; Collaborate with expert committees; Collaborate with internal partners; Collaborate with external partners; Collaborate with Study Team; Collaborate with monitoring team
Communication Scope
Verbal communication; Written communication; Presentation skills
Process & Methodology
Risk management, Manage multiple tasks, Prioritize tasks, Execute action plans
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