Sanofi
Senior Clinical Research Director, Ophthalmology
Sanofi, Convent Station, New Jersey, us, 07961
Senior Clinical Research Director, Ophthalmology
Join to apply for the Senior Clinical Research Director, Ophthalmology role at Sanofi.
Base pay range:
$225,000.00/yr - $375,000.00/yr
Job Title:
Senior Clinical Research 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 Senior Clinical Research Director (CRD) is an expert clinical lead for one or several indications in the Development of an R&D program and is responsible for leading clinical team(s) to deliver successful clinical trials for novel therapeutics for Ophthalmologic Diseases. The role requires clinical leadership, organization skills, strategically and operationally focused, resourceful individual with capacity to arbitrate to create synergies within the team and with external stakeholders, very good emotional intelligence, self‑motivation, solid analytical skills, and the ability deliver to multiple operational tasks.
We are looking for individuals with drive, curiosity, scientific mindset, and appreciation of teamwork with a diverse group of internal and external experts.
Main Responsibilities
Provide ophthalmology focused medical and scientific expertise to the cross‑functional project team to conduct the clinical studies from early phases to LCM programs
Establish clinical development strategy and lead clinical team, collaborate with other medical and clinical scientific experts, clinical development scientists in the project in collaboration with the Safety Officer, Regulatory Strategist, Statistics and other key functional representatives to deliver development strategy and prepare/assist with regulatory agency interactions
Develop or contribute to the regulatory documentation for the project(s), provide clinical leadership to other operational development activities pertaining to study start‑up (e.g. pressure test, competitive intelligence, patient engagement, cluster feasibility, study risk assessment)
Provide appropriate medical input & clinical leadership for all activities related to study conduct such as responses to IRBs and HA questions, protocol scientific and medical training, medical review of data within the scope of the centralized monitoring, clinical and medical information for the study team, medical advisors/Clinical Project Leaders from Clinical Study Units, and investigators
Responsible for the clinical part of regulatory documents, Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA) and answers to questions from health authorities.
Serve as the medical expert in the Clinical Study team, ensuring the medical relevance of the clinical data and able to act as mentor for other clinical team members, has the capacity to train them on the medical/scientific strategy by indication
Other Responsibilities
Designs the global clinical development strategy and generates the Clinical Development Plan (in close cooperation with other members of the team, particularly Regulatory Affairs and Health Economics); adjusts and updates the strategy according to the project progression and information available
Leads the clinical development including planned life cycle management (LCM)
Ongoing assessment of the product benefit‑risk profile during development and LCM, in strong collaboration with pharmacovigilance and clinical operations team
Implements strategies to identify, monitor and resolve clinical program/trial issues.
Responsible for medical monitoring for a study or clinical program as well as reviewing and monitoring study data.
Provide appropriate medical input & support for all activities related to clinical studies such as medical training, feasibility, medical review of data, documents, medical information/communications for the study team and other stakeholders
Prepares/reviews key clinical documents such as: meeting requests and briefing packages for Regulatory agencies, extended synopsis/protocol for clinical trials, Investigator Brochure, Clinical Trial Authorization dossier (IMPD, IND), summary of clinical efficacy and clinical overview of the Common Technical Document (CTD).
Provides clinical input to Statistical Analysis Plans (SAP), Target Product Profile (TPP) and Risk Management Plan
Writes/reviews answers to clinical questions from Health Authorities and IRB/Ethics Committees and investigators
Reviews Key Results Memos, Clinical Study Reports as well as scientific publications and communications on the project
Lead the medical/clinical assessment of license‑in opportunities, as needed
Manage other study physicians (CRDs) and clinical scientists in the same program, as needed
Author or co‑author manuscripts and abstracts
Establishes and maintains appropriate collaborations with key opinion leaders or advisory boards
Serves as clinical team leader/representative at the global project team(s), regulatory agency meetings, Steering committees, benefit‑risk assessment committee, and at the submission task force.
Scientific And Technical Expertise
Has and maintains deep scientific, technical, and clinical expertise in ophthalmology and retinal diseases
Understands and keeps updated with the pre‑clinical, clinical pharmacology and data relevant to the molecule of interest
Critically reads and evaluates relevant medical literature with deep understanding of the data and status from competitive products
Maintains visibility within the therapeutic area to maintain credibility with internal and external stakeholders
About You – Basic Qualifications
Medical Doctor (MD) and ophthalmology residency training required, fellowship training highly preferred
Minimum 5 years of clinical trial and/or clinical development experience
Fluent in English (verbal and written)
Preferred Qualifications
Board certified or eligible in Ophthalmology
Strong scientific and academic background with deep understanding of retina and eye diseases
Clinical trial or pharmaceutical experience in ophthalmology
Knowledge of drug development, ocular gene therapy, regulatory strategy
Good networking ability in cross‑cultural environment
Strong interpersonal, communication, presentation, and negotiation skills across all levels of the organization
Performance oriented with ability to work along agreed timelines and a focus on strategy and execution
Outstanding communicator. Excellent problem‑solving, conflict‑resolution and decision‑making 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.
Seniority level Director
Employment type Full‑time
Job function Research, Analyst, and Information Technology
Industries Pharmaceutical Manufacturing
Equal Opportunity Statement 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.
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. Sanofi US endeavors to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please click here.
Pursue Progress Discover Extraordinary. Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never‑been‑done‑before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s pursue progress and discover extraordinary – together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
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Base pay range:
$225,000.00/yr - $375,000.00/yr
Job Title:
Senior Clinical Research 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 Senior Clinical Research Director (CRD) is an expert clinical lead for one or several indications in the Development of an R&D program and is responsible for leading clinical team(s) to deliver successful clinical trials for novel therapeutics for Ophthalmologic Diseases. The role requires clinical leadership, organization skills, strategically and operationally focused, resourceful individual with capacity to arbitrate to create synergies within the team and with external stakeholders, very good emotional intelligence, self‑motivation, solid analytical skills, and the ability deliver to multiple operational tasks.
We are looking for individuals with drive, curiosity, scientific mindset, and appreciation of teamwork with a diverse group of internal and external experts.
Main Responsibilities
Provide ophthalmology focused medical and scientific expertise to the cross‑functional project team to conduct the clinical studies from early phases to LCM programs
Establish clinical development strategy and lead clinical team, collaborate with other medical and clinical scientific experts, clinical development scientists in the project in collaboration with the Safety Officer, Regulatory Strategist, Statistics and other key functional representatives to deliver development strategy and prepare/assist with regulatory agency interactions
Develop or contribute to the regulatory documentation for the project(s), provide clinical leadership to other operational development activities pertaining to study start‑up (e.g. pressure test, competitive intelligence, patient engagement, cluster feasibility, study risk assessment)
Provide appropriate medical input & clinical leadership for all activities related to study conduct such as responses to IRBs and HA questions, protocol scientific and medical training, medical review of data within the scope of the centralized monitoring, clinical and medical information for the study team, medical advisors/Clinical Project Leaders from Clinical Study Units, and investigators
Responsible for the clinical part of regulatory documents, Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA) and answers to questions from health authorities.
Serve as the medical expert in the Clinical Study team, ensuring the medical relevance of the clinical data and able to act as mentor for other clinical team members, has the capacity to train them on the medical/scientific strategy by indication
Other Responsibilities
Designs the global clinical development strategy and generates the Clinical Development Plan (in close cooperation with other members of the team, particularly Regulatory Affairs and Health Economics); adjusts and updates the strategy according to the project progression and information available
Leads the clinical development including planned life cycle management (LCM)
Ongoing assessment of the product benefit‑risk profile during development and LCM, in strong collaboration with pharmacovigilance and clinical operations team
Implements strategies to identify, monitor and resolve clinical program/trial issues.
Responsible for medical monitoring for a study or clinical program as well as reviewing and monitoring study data.
Provide appropriate medical input & support for all activities related to clinical studies such as medical training, feasibility, medical review of data, documents, medical information/communications for the study team and other stakeholders
Prepares/reviews key clinical documents such as: meeting requests and briefing packages for Regulatory agencies, extended synopsis/protocol for clinical trials, Investigator Brochure, Clinical Trial Authorization dossier (IMPD, IND), summary of clinical efficacy and clinical overview of the Common Technical Document (CTD).
Provides clinical input to Statistical Analysis Plans (SAP), Target Product Profile (TPP) and Risk Management Plan
Writes/reviews answers to clinical questions from Health Authorities and IRB/Ethics Committees and investigators
Reviews Key Results Memos, Clinical Study Reports as well as scientific publications and communications on the project
Lead the medical/clinical assessment of license‑in opportunities, as needed
Manage other study physicians (CRDs) and clinical scientists in the same program, as needed
Author or co‑author manuscripts and abstracts
Establishes and maintains appropriate collaborations with key opinion leaders or advisory boards
Serves as clinical team leader/representative at the global project team(s), regulatory agency meetings, Steering committees, benefit‑risk assessment committee, and at the submission task force.
Scientific And Technical Expertise
Has and maintains deep scientific, technical, and clinical expertise in ophthalmology and retinal diseases
Understands and keeps updated with the pre‑clinical, clinical pharmacology and data relevant to the molecule of interest
Critically reads and evaluates relevant medical literature with deep understanding of the data and status from competitive products
Maintains visibility within the therapeutic area to maintain credibility with internal and external stakeholders
About You – Basic Qualifications
Medical Doctor (MD) and ophthalmology residency training required, fellowship training highly preferred
Minimum 5 years of clinical trial and/or clinical development experience
Fluent in English (verbal and written)
Preferred Qualifications
Board certified or eligible in Ophthalmology
Strong scientific and academic background with deep understanding of retina and eye diseases
Clinical trial or pharmaceutical experience in ophthalmology
Knowledge of drug development, ocular gene therapy, regulatory strategy
Good networking ability in cross‑cultural environment
Strong interpersonal, communication, presentation, and negotiation skills across all levels of the organization
Performance oriented with ability to work along agreed timelines and a focus on strategy and execution
Outstanding communicator. Excellent problem‑solving, conflict‑resolution and decision‑making 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.
Seniority level Director
Employment type Full‑time
Job function Research, Analyst, and Information Technology
Industries Pharmaceutical Manufacturing
Equal Opportunity Statement 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.
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. Sanofi US endeavors to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please click here.
Pursue Progress Discover Extraordinary. Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never‑been‑done‑before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s pursue progress and discover extraordinary – together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
#J-18808-Ljbffr