Development Scientific Director, Ophthalmology
Company: Sanofi
Location: Cambridge
Posted on: January 12, 2026
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Job Description:
Job Title: Development Scientific Director Location: Morristown,
NJ Cambridge, MA About the Job Join the engine of Sanofi’s mission
— where deep immunoscience meets bold, AI-powered research. In
R&D, you’ll drive breakthroughs that could turn the impossible
into possible for millions. The Development Scientific Director
(DSD) is a responsible member of the clinical team dedicated to the
development and execution of clinical strategies and the clinical
and operational implementation of a complex compound program. The
primary purpose of the development scientific director’s position
is to support the Clinical Research Director (CRD) and/or clinical
lead in the medical/scientific contribution for the clinical
studies on activities pertaining to the Study Medical Manager (SMM)
responsibilities e.g.: leading or contributing to key study
documents and activities from clinical development plans and trial
set-up to clinical study report in compliance with quality and
regulatory processes. About Sanofi: We’re an R&D-driven,
AI-powered biopharma company committed to improving people’s lives
and delivering compelling growth. Our deep understanding of the
immune system – and innovative pipeline – enables us to invent
medicines and vaccines that treat and protect millions of people
around the world. Together, we chase the miracles of science to
improve people’s lives. Main Responsibilities: Development
scientific director provides active scientific contribution to a
cross-functional clinical team developing a molecular entity,
provide input to the clinical development plan, work on the
development of the clinical trial protocol , clinical trial
materials, and take responsibility for coordinating completion of
clinical study reports and support preparation of relevant
documents for regulatory filings. This role will involve extensive
team matrix interactions with colleagues from a number of different
disciplines and development scientist is responsible for leading or
representing clinical development across specific aspects of
clinical trial execution. This individual may be asked to
contribute to the evaluation of scientific opportunities in the
therapeutic area. Under the guidance of his/her manager in the
Therapeutic Area department, he/she collaborates with the Coding
specialist, Biostatisticians, Data Managers, Global and Regional
Study Managers, Feasibility Managers, Pharmacovigilance
representative, Medical Writer (e.g. planning and review of
narratives) on high quality medical scientific documents, as
needed. He/she ensures appropriate review and consistency of the
data and investigations of safety cases with the Clinical Trial
Team (Monitoring Teams) or Pharmacovigilance. About You Knowledge
And Skills Required : Ophthalmology/retina clinical development,
clinical trial methodology knowledge and experience required
Leadership skills to give directions and organize the activities on
behalf of the CRD Scientific expertise or interest and ability to
learn in the domain of assigned study/project. Ability to
synthesize the scientific information, excellent presentation
skills Experience in drafting protocols/amendments, providing input
to CSRs, regulatory documents (IBs/ INDs, Briefing books etc.)
Familiar with digital tools such as data analytics or agility to
use them Quality focused, able to develop good practices, using a
critical data-driven and risk management approach Ability to work
autonomously and efficiently to provide status reports and to
anticipate and escalate issues in a timely manner to execute action
plans Well organized, high level of autonomy and motivation, Good
communication skills (verbal and written) Multiple tasks handling
and prioritization Able to make proposals to manage challenging
situations Ability to work in project mode with study team and CRDs
and develop trust and effectiveness Management of priorities and
workload, if involved in several projects Ability to develop strong
leadership and collaborate with cross functional team members Team
and results oriented Experience of working internationally with
Strong English skills (verbal and written if English is not the
native language) This position may require up to 15% travel Formal
Education And/Or Experience Required: Ph.D. preferred, Masters
degree considered for candidates with extensive experience. A
minimum of 3 years of phase I-III clinical trial/drug development
experience within the ophthalmology/retina pharmaceutical industry
or CRO is required Knowledge in ICH, GCP. Fluent in English.
Knowledge And Skills Desirable But Not Essential: Global trial
experience Clinical operations, Statistical, data management
Regulatory knowledge 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.
GD-SA LI-SA LI-Onsite vhd All compensation will be determined
commensurate with demonstrated experience. Employees may be
eligible to participate in Company employee benefit programs, and
additional benefits information can be found here.
Keywords: Sanofi, Fall River , Development Scientific Director, Ophthalmology, Science, Research & Development , Cambridge, Massachusetts
