The Senior Manager - Medical Reviews leads the evaluation and approval of medical and promotional materials within the Rare Blood Disorders franchise to ensure compliance with FDA regulations and corporate policies. This role involves providing strategic and scientific expertise to support effective drug promotion and labeling, minimizing regulatory risks while optimizing patient care outcomes. The position requires strong communication skills, critical thinking, and deep knowledge of clinical and regulatory standards in the pharmaceutical industry.
Job Title: Senior Manager - Medical Reviews
Location : Cambridge, MA
About the Job
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress.
The Senior Manager, Medical Review is a Cambridge-based member of the US Medical team in the Rare Blood Disorders franchise covering portfolio. The mission of this team is to support the company by functioning as the internal expert in rare blood disorders and therapies and helping Health Care Professionals and Payers optimize patient care and treatment outcomes through evidence-based decisions. We feel this is best accomplished through the generation, interpretation and communication of accurate clinical and scientific information. The Senior Manager plays a key role in this mission by providing strategic input into the rare blood portfolio and reports to the Director of Medical Operations.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
The Senior Manager of Medical Reviews will:
Ensure timely Medical Material and Promotional Material reviews via the Medical Material Review Committee (MMRC) and Promotional Review Board (PRB).
Ensure full compliance with all corporate and industry policies and legal and regulatory requirements, for all medical affairs activities
Ensure promotional/non-promotional review for assigned products in the RBD BU, which include major assets, sound medical advice that minimizes the risk of regulatory and legal action, competitively positions assigned products and is consistent with applicable FDA regulations and company policies for advertising and promotion of prescription drug products and biologics
Provision of competitively positioned promotional materials that comply with applicable FDA and corporate regulations, policies and guidance
Analyze whether clinical and non-clinical promotional claims are supported
Provide insight, judgment and sound decisions on promotional programs and tactics for assigned products.
Maintain a deep and current awareness of evolving FDA regulations and interpretations, FDA advisory comments, enforcement letters and policy issues affecting the pharmaceutical/biologics industry and communicate relevant information appropriately to stakeholders.
Advise on the development of US labeling to ensure support for anticipated promotional messages and claims.
Develop/maintain an in-depth understanding of labeling for assigned company and competitor products and the subsequent translation of that knowledge into the development of promotional materials.
• Ensure application of key learnings across assigned brands, ensuring alignment of development and commercial objectives
• With limited supervision, recommend appropriate actions for proposed advertising and promotion sometimes with little or no precedent
Develop/maintain an in-depth understanding of labeling for assigned company and competitor products and the subsequent translation of that knowledge into the development of promotional materials.
About You
Qualifications:
Advanced degree (PhD, PharmD, MD) required
Previous experience in medical review or ad-promo either in industry or agency highly preferred
Demonstrated detailed orientated and strong attention to data accuracy and consistency
Be hands-on and accountable
Possess outstanding communication and influencing skills, able to work in a multi-cultural environment, and represent the company with utmost professionalism in a wide array of forums
Be a critical thinker, able to share fact-based opinions
Able to make complex science understandable for a non-scientific audience
Results-oriented, can embrace a fast-paced “can do” culture undefined
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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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information canbe found here.
medical review, pharmaceutical compliance, FDA regulations, promotional material review, rare blood disorders, clinical research, drug development, medical affairs, labeling compliance, regulatory affairs