Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.
Our Team:
The Lunsekimig project team is part of Early Development in the Inflammation & Immunology Therapeutic Area at Sanofi. Our team is developing a novel pentavalent, bispecific Nanobody for the treatment of asthma and other "Type 2" inflammatory diseases. We are currently aggressively growing our team to support our high priority expansion into several high prevalence/high impact diseases with multiple trial starts in the next 12 months. This includes the initiation of replicate phase 3 clinical trials in the respiratory space.
Main Responsibilities:
The lunsekimig team is seeking an experienced clinical scientist for the role of senior Clinical Scientist. The primary purpose of the Senior Clinical Scientist's position is to assist/support the Clinical Research Director (CRD) in the medical/scientific contribution for the clinical studies, on activities pertaining to the Study Medical Manager responsibilities e.g.: managing or contributing to the operational activities from clinical trial set-up to clinical study report in compliance with quality and regulatory processes.
Strategic clinical development plans:
Contributes to preparation and/or review of any documents related to the studies and requiring a scientific background (abbreviated protocol/protocol/amended protocol, patient written information, presentations/communication to internal or external partners, study reports, committee charters, protocol registration form, redacted protocol, lay summary...)
Supports CRD in the preparation of medical answers to questions from Health Authorities, IRB/Ethics Committees, investigators, experts involved in the study/project
Contributes to the definition of the critical data/processes/predefined deviations list, risks and Quality tolerance limits identification and monitoring, to implement/develop related sections of the study risk management plan
Support the Clinical Lead and CRD to prepare presentations to obtain endorsement of the clinical strategic plan with the appropriate governance committees
Support the design and execution of multiple clinical studies defined within development plan
Support the preparation of key clinical documents to be prepared for clinical trials (protocols, informed consent, charters, benefit risk assessments)
Team development
Support CRDs and Clinical Lead in onboarding, training, and support of Clinical Scientists and other team members
Support CRDs, Clinical Lead and Global Project Head with cross-programs strategy and activities
Maintain deep scientific, technical, and clinical expertise in immunology, dermatology, pulmonology, or other disease areas within the Immunology and Inflammation therapeutic area
Skills that you have (mandatory):
Advanced degree preferred (PharmD or PhD scientist and Biomedical Science master is a plus)
5+ years of industry experience (including both research and clinical development)
1+ years experience as clinical scientist
Proficient in clinical literature and critical interpretation of clinical study results
Experience with supporting preparation and execution of clinical trials
Open, transparent, collaborative working style
Good leadership, interpersonal, communication, and presentation skills
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
