Senior Clinical Research Director, Rare
Location:
Cambridge, MA or Morristown, NJ
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.
As the Senior Clinical Research Director (Senior CRD) within the RARE Therapeutic Area, you will be the expert clinical lead for one or several indications in the Development of an R&D program. The role requires medical leadership, organization skills and a strategically and operationally focused, resourceful individual. The Senior CRD shows 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 to deliver multiple operational tasks.
To support sustainable growth, Sanofi Global Development ambition is to be the industry‑leading Development organization, using impactful therapeutic innovation that turns hope into reality for people. The RARE Therapeutic Area leads the development of therapies for rare inherited disorders by overseeing the portfolio of development projects and execution of the development programs through the multi‑disciplinary Global Project Team (GPT). The Rare Neurometabolic Cluster oversees development projects and execution of the development programs of lysosomal storage with systemic and neurological manifestations, neuromuscular and neurodevelopmental disorders.
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.
Main Responsibilities
Provide medical expertise in the Study team to conduct the clinical studies from early phases to LCM programs.
Collaborate with other medical and clinical scientific experts (CRDs or DSDs) in the project under the leadership of the Global Project Head, with the Global Safety Officer, Regulatory Strategist and other key functional representatives to deliver development strategy and prepare/assist with regulatory bodies interaction.
Develop the study‑level regulatory documentation (Abbreviated Protocol, Protocol, Amended protocol) for their project, lead 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 & support for all activities related to clinical studies conduct such as answers 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.
Develop the clinical part of Briefing regulatory documents, Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA, etc.) and answers to questions from health authorities.
Be the medical reference in the Clinical Study team, ensuring the medical relevance of the clinical data and act as mentor for other DMDs/DSDs/CSs, train them on the medical/scientific strategy by indication.
Key Responsibilities Include Leading the clinical development plan strategies:
Responsible for the clinical development plans and clinical sections of integrated development plans (IDP).
Contribute in the definition of the product value proposition (TVP), Target Product Profile (TPP) and market access strategy (in collaboration with respective functions) and the focus of the research strategy, by providing input on existing clinical needs and approaches to clinical development strategies for research projects.
Prepare Internal Governance documents and contribute to the medical aspects of the TPP, TVP and other GPT documents related to one or several indications of the IDP in support of the GPH.
Collaborate with other DMDs/DSDs within the project, ensure leadership, build consensus, coordinate action plans with stakeholders to resolve project‑related issues, anticipate potential issues and share lessons learned across the project or study teams.
Raise study or project‑level issues to the project head and propose related corrective action plans.
Collaborate with external partners, regulators, scientific experts and internal stakeholders.
Provide operational expertise to project clinical sub team, as needed.
Evaluate relevant medical literature and status from competitive products.
Lead, Support and oversee the execution of clinical development and studies activities
Collaborate and communicate appropriately with all function stakeholders (e.g. clinical operations, project management, Patient Safety, Pharmacovigilance, regulatory, Finance, Scientific External Engagement, Procurement, etc.), responsible for timelines, budgets and contingency/risk management plans to assure successful execution of the clinical trials in compliance with Good Clinical Practice (GCP), applicable laws and regulations and applicable standard operating procedures (SOPs).
Develop the abbreviated protocol, the final protocol and protocol amendments.
Develop/review the Core Study Informed Consent Form (CSICF).
Develop/review Study Committee Charters.
Collaborate on key medical and clinical questions with the Global feasibility manager to prepare and interpret feasibility and competitive intelligence results.
Review and provide clinical input across different study documents (Vendors RFPs, (e)CRF, (e) diary, (e)CoA, etc.).
Provide medical/clinical input to study‑related documents such as study plans (Study risk management plan, Monitoring and centralised monitoring plans).
Participate in the elaboration of training material and presentations at the investigator meetings/local teams trainings.
Answer to medical questions raised by HA, EC/IRBs, sites.
Ensure quality of clinical data through continuous data validation, blinded data review on summary tables or electronic data visualisation during clinical trial conduct (AE dedicated review, and Clinical Case review for safety data and statistical surveillance for efficacy data).
Ensure trial master file documents readiness and availability, and mandatory trainings linked to the clinical function.
Lead the study‑specific committees (IDMC, steering committees, adjudication) with operational support.
Co‑Develop the SAP in collaboration with biostats.
Responsible for key results preparation.
Develop/Review the clinical study report.
Responsibilities Related To Regulatory And Safety Documents And Meetings
Represent project in interactions with regulatory bodies, lead strategy and write clinical sections of the CTD, briefing docs and support registration, labelling, etc.
Develop and/or contribute in the clinical section of the Investigator’s brochure, CTA, IND, DSUR, DRMP, RMP.
Contribute in the clinical sections of the BLA/CTD, Briefing packages for regulatory meetings, PSP/PIP.
Ensure clinical data meets all necessary regulatory standards.
Collaborate with the Patient Safety GSO to detect and document any safety signal.
Participate in Advisory Committee preparation.
Scientific Data Evaluation And Authorship
Participate and author manuscripts and abstracts.
Establish and maintain appropriate collaborations with knowledge experts or advisory boards.
Represent medical function on an ad‑hoc basis for specific tasks such as the evaluation of potential in‑licencing candidates for the therapeutic area and serve as the clinical advisor to research teams.
Experience
At least 4 years previous experience in clinical development in the pharmaceutical industry or a CRO or medical experience in clinical development in a healthcare institution.
Soft Skills
Very good communication skills (verbal and written) for interactions across functional areas and with key regulatory agencies.
Excellent problem‑solving capability.
Demonstrated capability to challenge decision and status‑quo with a risk‑management approach.
Quality‑focused, able to develop good practices, using a critical data‑driven and risk‑management approach.
Multiple tasks handling and prioritization.
Ability to negotiate to ensure operational resources are available for continued clinical conduct.
Mentoring skills and evaluation of resources performance capability.
Ability to work within a matrix model.
International/intercultural working skills.
Open‑minded to apply new digital solutions.
Technical Skills
Understanding of pharmaceutical product development and life cycle management.
Very good scientific and medical/clinical expertise.
Very good expertise in clinical development and methodology of clinical studies.
Acquired expertise (by training or experience) in interaction with Health Authorities.
Education
Medical Doctor (MD) preferred: GP or specialist; training in pediatrics or pediatric neurology is a plus.
Languages
English fluent (spoken and written).
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 recognises 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 programmes and at least 14 weeks’ gender‑neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affidivite Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race, colour, 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, 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.
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Location:
Cambridge, MA or Morristown, NJ
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.
As the Senior Clinical Research Director (Senior CRD) within the RARE Therapeutic Area, you will be the expert clinical lead for one or several indications in the Development of an R&D program. The role requires medical leadership, organization skills and a strategically and operationally focused, resourceful individual. The Senior CRD shows 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 to deliver multiple operational tasks.
To support sustainable growth, Sanofi Global Development ambition is to be the industry‑leading Development organization, using impactful therapeutic innovation that turns hope into reality for people. The RARE Therapeutic Area leads the development of therapies for rare inherited disorders by overseeing the portfolio of development projects and execution of the development programs through the multi‑disciplinary Global Project Team (GPT). The Rare Neurometabolic Cluster oversees development projects and execution of the development programs of lysosomal storage with systemic and neurological manifestations, neuromuscular and neurodevelopmental disorders.
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.
Main Responsibilities
Provide medical expertise in the Study team to conduct the clinical studies from early phases to LCM programs.
Collaborate with other medical and clinical scientific experts (CRDs or DSDs) in the project under the leadership of the Global Project Head, with the Global Safety Officer, Regulatory Strategist and other key functional representatives to deliver development strategy and prepare/assist with regulatory bodies interaction.
Develop the study‑level regulatory documentation (Abbreviated Protocol, Protocol, Amended protocol) for their project, lead 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 & support for all activities related to clinical studies conduct such as answers 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.
Develop the clinical part of Briefing regulatory documents, Common Technical Document for submission to regulatory bodies (FDA, EMA, PMDA, etc.) and answers to questions from health authorities.
Be the medical reference in the Clinical Study team, ensuring the medical relevance of the clinical data and act as mentor for other DMDs/DSDs/CSs, train them on the medical/scientific strategy by indication.
Key Responsibilities Include Leading the clinical development plan strategies:
Responsible for the clinical development plans and clinical sections of integrated development plans (IDP).
Contribute in the definition of the product value proposition (TVP), Target Product Profile (TPP) and market access strategy (in collaboration with respective functions) and the focus of the research strategy, by providing input on existing clinical needs and approaches to clinical development strategies for research projects.
Prepare Internal Governance documents and contribute to the medical aspects of the TPP, TVP and other GPT documents related to one or several indications of the IDP in support of the GPH.
Collaborate with other DMDs/DSDs within the project, ensure leadership, build consensus, coordinate action plans with stakeholders to resolve project‑related issues, anticipate potential issues and share lessons learned across the project or study teams.
Raise study or project‑level issues to the project head and propose related corrective action plans.
Collaborate with external partners, regulators, scientific experts and internal stakeholders.
Provide operational expertise to project clinical sub team, as needed.
Evaluate relevant medical literature and status from competitive products.
Lead, Support and oversee the execution of clinical development and studies activities
Collaborate and communicate appropriately with all function stakeholders (e.g. clinical operations, project management, Patient Safety, Pharmacovigilance, regulatory, Finance, Scientific External Engagement, Procurement, etc.), responsible for timelines, budgets and contingency/risk management plans to assure successful execution of the clinical trials in compliance with Good Clinical Practice (GCP), applicable laws and regulations and applicable standard operating procedures (SOPs).
Develop the abbreviated protocol, the final protocol and protocol amendments.
Develop/review the Core Study Informed Consent Form (CSICF).
Develop/review Study Committee Charters.
Collaborate on key medical and clinical questions with the Global feasibility manager to prepare and interpret feasibility and competitive intelligence results.
Review and provide clinical input across different study documents (Vendors RFPs, (e)CRF, (e) diary, (e)CoA, etc.).
Provide medical/clinical input to study‑related documents such as study plans (Study risk management plan, Monitoring and centralised monitoring plans).
Participate in the elaboration of training material and presentations at the investigator meetings/local teams trainings.
Answer to medical questions raised by HA, EC/IRBs, sites.
Ensure quality of clinical data through continuous data validation, blinded data review on summary tables or electronic data visualisation during clinical trial conduct (AE dedicated review, and Clinical Case review for safety data and statistical surveillance for efficacy data).
Ensure trial master file documents readiness and availability, and mandatory trainings linked to the clinical function.
Lead the study‑specific committees (IDMC, steering committees, adjudication) with operational support.
Co‑Develop the SAP in collaboration with biostats.
Responsible for key results preparation.
Develop/Review the clinical study report.
Responsibilities Related To Regulatory And Safety Documents And Meetings
Represent project in interactions with regulatory bodies, lead strategy and write clinical sections of the CTD, briefing docs and support registration, labelling, etc.
Develop and/or contribute in the clinical section of the Investigator’s brochure, CTA, IND, DSUR, DRMP, RMP.
Contribute in the clinical sections of the BLA/CTD, Briefing packages for regulatory meetings, PSP/PIP.
Ensure clinical data meets all necessary regulatory standards.
Collaborate with the Patient Safety GSO to detect and document any safety signal.
Participate in Advisory Committee preparation.
Scientific Data Evaluation And Authorship
Participate and author manuscripts and abstracts.
Establish and maintain appropriate collaborations with knowledge experts or advisory boards.
Represent medical function on an ad‑hoc basis for specific tasks such as the evaluation of potential in‑licencing candidates for the therapeutic area and serve as the clinical advisor to research teams.
Experience
At least 4 years previous experience in clinical development in the pharmaceutical industry or a CRO or medical experience in clinical development in a healthcare institution.
Soft Skills
Very good communication skills (verbal and written) for interactions across functional areas and with key regulatory agencies.
Excellent problem‑solving capability.
Demonstrated capability to challenge decision and status‑quo with a risk‑management approach.
Quality‑focused, able to develop good practices, using a critical data‑driven and risk‑management approach.
Multiple tasks handling and prioritization.
Ability to negotiate to ensure operational resources are available for continued clinical conduct.
Mentoring skills and evaluation of resources performance capability.
Ability to work within a matrix model.
International/intercultural working skills.
Open‑minded to apply new digital solutions.
Technical Skills
Understanding of pharmaceutical product development and life cycle management.
Very good scientific and medical/clinical expertise.
Very good expertise in clinical development and methodology of clinical studies.
Acquired expertise (by training or experience) in interaction with Health Authorities.
Education
Medical Doctor (MD) preferred: GP or specialist; training in pediatrics or pediatric neurology is a plus.
Languages
English fluent (spoken and written).
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 recognises 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 programmes and at least 14 weeks’ gender‑neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affidivite Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race, colour, 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, 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.
#J-18808-Ljbffr