Sanofi Group
Director Clinical Development
Sanofi Group, Convent Station, New Jersey, us, 07961
Sanofi Group Director Clinical Development Morristown, New Jersey Apply Now
Location:
Swiftwater, PA, Cambridge, MA, Orlando, FL or Morristown, NJ site (flexibility with US site)About the jobWe 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. 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.The Director Clinical Development is the clinical/medical/scientific expert who supports the translation of a target product profile into a feasible Clinical Development Plan (CDP), considering scientific environment, resource possibilities, clinical feasibility, and timely execution. This requires a good understanding of the operational environment, team leadership skills, communication skills, knowledge of the therapeutic area, and the ability to translate business needs into feasible operational plans.Main responsibilitiesProvide scientific and clinical leadership in the design and development of clinical studies and programs for Sanofi Vaccines R&D.Have global responsibility and ownership for the Clinical Strategy, the respective Clinical Development Plans (CDP), and study protocols for projects/programs.Ensure that CDPs are written in accordance with the Target Product Profile (TPP), Integrated Evidence Generation Plan (IEGP), and Franchise and Global Project Team strategy, assuring global consistency across regions.Provide clinical and R&D expertise, guidance, and direction in the context of the region/country in which they operate.Establish the conditions essential for determining the safety of all subjects involved in Clinical trials for the vaccine development candidates they oversee.Provide clinical expertise and support to regulatory activities (Health Authority meetings, communications, CTD submissions).About youYou will lead the clinical study team and require leadership skills, communication skills, the ability to operate in multidisciplinary and multi-cultural teams, and the ability to inspire teams.Physician, with training in Infectious Diseases, Geriatrics, Pediatrics, or Internal Medicine, in addition to training or experience in immunology, preferred. MD is a minimum scientific qualification.5-10 years of pharmaceutical industry experience preferred, with exposure to diverse programs in early and late-stage development or more experience conducting early and late-stage clinical trials in an academic environment.Demonstrated scientific productivity (publications, research reports, etc.) and ability to critically review/interpret research data, preferred.Demonstrated planning, organizational skills, interpersonal, problem-solving, and excellent written and verbal communication skills.Ability to work independently across many interfaces and platforms in a matrix, cross-cultural environment is essential.M.D. with completion of an approved residency training program in a related field or equivalent is preferred.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.
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Location:
Swiftwater, PA, Cambridge, MA, Orlando, FL or Morristown, NJ site (flexibility with US site)About the jobWe 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. 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.The Director Clinical Development is the clinical/medical/scientific expert who supports the translation of a target product profile into a feasible Clinical Development Plan (CDP), considering scientific environment, resource possibilities, clinical feasibility, and timely execution. This requires a good understanding of the operational environment, team leadership skills, communication skills, knowledge of the therapeutic area, and the ability to translate business needs into feasible operational plans.Main responsibilitiesProvide scientific and clinical leadership in the design and development of clinical studies and programs for Sanofi Vaccines R&D.Have global responsibility and ownership for the Clinical Strategy, the respective Clinical Development Plans (CDP), and study protocols for projects/programs.Ensure that CDPs are written in accordance with the Target Product Profile (TPP), Integrated Evidence Generation Plan (IEGP), and Franchise and Global Project Team strategy, assuring global consistency across regions.Provide clinical and R&D expertise, guidance, and direction in the context of the region/country in which they operate.Establish the conditions essential for determining the safety of all subjects involved in Clinical trials for the vaccine development candidates they oversee.Provide clinical expertise and support to regulatory activities (Health Authority meetings, communications, CTD submissions).About youYou will lead the clinical study team and require leadership skills, communication skills, the ability to operate in multidisciplinary and multi-cultural teams, and the ability to inspire teams.Physician, with training in Infectious Diseases, Geriatrics, Pediatrics, or Internal Medicine, in addition to training or experience in immunology, preferred. MD is a minimum scientific qualification.5-10 years of pharmaceutical industry experience preferred, with exposure to diverse programs in early and late-stage development or more experience conducting early and late-stage clinical trials in an academic environment.Demonstrated scientific productivity (publications, research reports, etc.) and ability to critically review/interpret research data, preferred.Demonstrated planning, organizational skills, interpersonal, problem-solving, and excellent written and verbal communication skills.Ability to work independently across many interfaces and platforms in a matrix, cross-cultural environment is essential.M.D. with completion of an approved residency training program in a related field or equivalent is preferred.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.
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