Rare Diseases Registries Head

Sanofi • Cambridge, MA

2d • Onsite

About The Position

Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you’ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs. The Rare Diseases (RD) Registries Operations and Engagement Lead is a critical global role contributing to the continued development and growth of the Rare Diseases Registry at Sanofi. The individual will be responsible for program coordination/management and operational leadership of the Rare Disease Registries. This role offers an opportunity to work on the cutting-edge Rare Diseases Patient registries across multiple Lysosomal Storage Diseases and contribute to the advancement of rare diseases patient research through real world data collection. The Rare Diseases (RD) Registries Operations and Engagement Lead reports to the Global Head for Medical Strategy, Planning and Innovation for Rare Diseases. This role requires a GLOCAL mindset and an innovative approach to problem solving but also rooted in the tradition and legacy of patient centricity. The Registries Operations and Engagement lead will also work closely with the individual TA Medical Heads and Medical Directors for Gaucher, Pompe and Fabry. This individual will also work in close collaboration with other members of the global, regional, affiliate, cross-functional, and alliance teams to enhance the growth of the RD franchise. 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. This position is based in Cambridge, Massachusetts.

Requirements

• Bachelors in relevant scientific or technical disciplines
• 5 - 10 years of work experience in pharma/relevant field (clinical trials/registry and/or project management experience a definite plus)
• Strong cross functional leadership and influencing skills. Ability to lead people, timelines, and work in a matrix organization in compliant and professional manner.
• Experience in managing quarterly budgets.
• Excellent presentation, writing, power point and organizational skills.
• Experience managing external vendors.
• Working knowledge of the regulatory environment.
• Experience in strategic development in a multi-dimensional and rapid changing environment.

Nice To Haves

• Advanced degree a plus
• Attention to detail and accuracy is a must
• Demonstrates good common sense and compassion
• Advanced knowledge and proficiency of Microsoft Applications including Excel, PowerPoint and Word
• Experience with the implementation of digital initiatives is a plus
• Experience with cross-functional teams and regional and country level counterparts
• Experience in managing vendors and external business partners
• International cross-cultural aptitude and experience is a plus
• An analytical mindset and problem-solving skills
• Ability to manage and coordinate multiple activities and shifting priorities
• Ability to meet deadlines
• Negotiation skills

Responsibilities

• Developing an overall strategic and operational plan for RD Registries
• Overseeing all RD registry projects and ensure compliance with global guidelines.
• Leading a team of Rare Disease Registry Operations professionals including Site Operations, Data Management and Programming .
• Developing, maintaining, and monitoring registry programs including tracking of cross functional project milestones/timelines and contracts management
• Ensuring that key Registries programs, e.g. registry-based studies, digital initiatives (e.g. eConsent, ePRO, etc), and para-registry programs are implemented and delivered on time with optimal resource management.
• Proactively identifying and progressing key para-registry opportunities for collaboration, data analysis and dissemination that are aligned with Registries/Global medical strategies
• Preparing for potentially new or external registries/partnerships (e.g. public private partnerships)
• Maintaining overall registries budget
• Creating reports and dashboards on a regular basis for monthly, quarterly and annual distribution
• Serving as a primary contact for ad-hoc requests from various Business Unit functions and Regional teams for registry data and information
• Liaising with vendors/collaborators as needed for implementation of key projects
• Communicating internal and external value proposition of RD Registry

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level