US Medical Lead, Solid Tumors (Apply in 3 Minutes) Position Available In Middlesex, Massachusetts

Job Description:

Job Title:

US Medical Lead, Solid Tumors Location:

Cambridge, MAAbout the Job The US Medical Lead, Solid Tumors, will play apivotal role in shaping the strategic direction and providingmedical leadership for the Solid Tumor Oncology portfolio with aspecific focus on Sanofi’s Radio-ligand therapy and the expectedlaunch in GEP-NET. This position will involve working closely withcross-functional teams to ensure the successful planning andexecution of medical affairs activities, clinical trials, andproduct support. This position will be part of the US OncologyMedical Leadership Team. US medical advance patient-centric medicalcapabilities and collaborative partnerships that differentiateSanofi in the Oncology communities, aiming to improve patientoutcomes by accelerating proper integration of our cutting-edgescience into US clinical practice. We are an innovative globalhealthcare company, committed to transforming the lives of peoplewith immune challenges, rare diseases and blood disorders, cancers,and neurological disorders. From R D to sales, our talentedteams work together, revolutionizing treatment, continuallyimproving products, understanding unmet needs, and connectingcommunities. We chase the miracles of science every single day,pursuing Progress to make a real impact on millions of patientsaround the world.

Main Responsibilities:

•

Strategic Leadership:

Set the vision and proactively shape the strategic direction forthe Solid Tumor Oncology portfolio, including products at variousstages of development.

• Medical Affairs Expertise:

  Provide medicalaffairs expertise for solid tumor oncology products, adjustinginput based on the stage of development.

• Cross-functionalCollaboration:

  Lead a cross-functional team of medicalprofessionals in planning and executing all aspects of medicalaffairs, including medical science, clinical trials, marketingstrategies, and key publications.

• Regulatory and ComplianceOversight:

  Oversee the medical review and approval of regulatorydocuments, ensuring adherence to company standards andgovernment/industry regulations.

• Clinical Trial ProgramManagement:

  Oversee the US medical affairs Solid Tumor Oncologyclinical trial program, ensuring strategic development of clinicaldata, including expanded access program

• Product Support:

  Providemedical support to product planning and LCM groups, includingimpact assessments of line extensions, new indications, andpublication strategies.

• Global Collaboration:

  Work withcolleagues in Global Medical Affairs and other markets to ensureconsistency of worldwide programs from a medical perspective.

• Joint Ventures Alignment:

  Assure alignment of initiatives acrossexisting Joint Ventures, including strategy and program execution

• Business Strategy Development:

  Ensure medical representation onProduct Business teams and Product Promotional Review teams,contributing to short and long-term business strategies andobjectives.

• KOL Engagement:

  Develop and maintain professionalrelationships with Key Opinion Leaders (KOLs) within the medicalcommunity. Oversee the establishment and maintenance of externalscientific advisory boards and assist in advocacy development.

•

Continuous Learning and Development:

Stay informed of currentdevelopments within the medical and scientific communities throughliterature, meetings, conventions, and professional associations.

About You Qualifications:

Education:

• Doctorate degree from anaccredited college or university (e.

g., M.D., PhD, PharmD, orequivalent) with experience in a medical oncology-related field.

Board certified/eligible in Oncology preferred.

Experience:

• Atleast 10 years of total experience post-degree, including clinicalpractice.
• At least 5 years of progressive experience in thepharmaceutical or biotech industry working in Medical Affairsand/or clinical research and development.
• Experience in planning,executing, and reporting clinical trials.
• At least 3 years ofexperience direct or matrix leading people and/or departments.
• Prior experience with solid tumor, radio-medicine, and/orneuroendocrine tumors preferred.

Skills:

• Extensive clinicalknowledge in Oncology.
• Strong interpersonal, verbal, and writtencommunication skills.
• Strong understanding of clinical trialsprocesses and FDA approval processes, including acceleratedapproval, and FDA and other regulations and guidance governingcommercial promotional material and medical scientific exchange.
• Experience with developing and executing US expanded accessprotocol
• Ability to build solid working relationships withcommercial organizations and influence across cultures.
• Demonstrated ability to organize and lead Clinical ResearchAdvisory Panels.
• Ability to work with and effectively supportcross-functional teams.
• Broad and formal leadership experience,including excellent “leadership presence” to represent MedicalAffairs within the company and to external stakeholders.

PersonalAttributes:

• Strong interpersonal skills with the ability toinfluence others.
• Excellence in problem-solving with superiorjudgment and a balanced, realistic understanding of issues.
• Ateam player with the ability to collaborate successfully with bothinternal and external colleagues.
• Strong analytical skills andcomfort managing through ambiguity.
• Ability to manage competingpriorities and projects, requiring excellent prioritization andexpectation management skills. Why Choose Us?
• Bring the miraclesof science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive yourcareer, whether it’s through a promotion or lateral move, at homeor internationally.
• Enjoy a thoughtful, well-crafted rewardspackage that recognizes your contribution and amplifies yourimpact.
• Take good care of yourself and your family, with a widerange of health and wellbeing benefits including high-qualityhealthcare, prevention and wellness programs and at least 14 weeks’gender-neutral parental leave.

Sanofi Inc. and its U.S. affiliatesare Equal Opportunity and Affirmative Action employers committed toa culturally diverse workforce. All qualified applicants willreceive 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 militarystatus; domestic violence victim status; atypical cellular or bloodtrait; genetic information (including the refusal to submit togenetic testing) or any other characteristic protected by law.

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LI-Onsite vhd All compensation will be determinedcommensurate with demonstrated experience. Employees may beeligible to participate in Company employee benefit programs, andadditional benefits information can be found here.