What are the responsibilities and job description for the Medical Information Specialist / Writer (Clinical) (contract) position at Sanofi?
Job Title: Medical Information Specialist / Writer II
Location: Hybrid (3 days on-site) - Morristown, NJ
Type: Contract (W2)
Term: 12-months
Schedule: Monday - Friday; 9 AM - 5 PM ET
Pay Rate Max: $64 per hour
Sanofi's contingent workforce program, FLEXT Direct, is seeking a Medical Information Specialist / Writer II for a 12-month contract.
This individual will join our Global Medical Information and Insights (MI&I) content team, supporting a dynamic portfolio spanning immunology, oncology, and neurology therapeutic areas. In this role, you will be responsible for ensuring the quality, accuracy, and integrity of medical information responses delivered to healthcare professionals and patients worldwide. Working under the direction of senior content leadership, you will contribute to the development and review of global medical information content, provide country and regional support, and collaborate cross-functionally with internal and external stakeholders across multiple global business units. This position demands a blend of deep scientific expertise, exceptional communication skills, and strong organizational capabilities to manage complex content workflows and support medical information activities across a broad and impactful product portfolio.
Responsibilities
Location: Hybrid (3 days on-site) - Morristown, NJ
Type: Contract (W2)
Term: 12-months
Schedule: Monday - Friday; 9 AM - 5 PM ET
Pay Rate Max: $64 per hour
Sanofi's contingent workforce program, FLEXT Direct, is seeking a Medical Information Specialist / Writer II for a 12-month contract.
This individual will join our Global Medical Information and Insights (MI&I) content team, supporting a dynamic portfolio spanning immunology, oncology, and neurology therapeutic areas. In this role, you will be responsible for ensuring the quality, accuracy, and integrity of medical information responses delivered to healthcare professionals and patients worldwide. Working under the direction of senior content leadership, you will contribute to the development and review of global medical information content, provide country and regional support, and collaborate cross-functionally with internal and external stakeholders across multiple global business units. This position demands a blend of deep scientific expertise, exceptional communication skills, and strong organizational capabilities to manage complex content workflows and support medical information activities across a broad and impactful product portfolio.
Responsibilities
- Write, review, and maintain high-quality global medical information response documents, including scientific response letters and standard response documents
- Review and manage escalations received from the medical information call center, ensuring timely and accurate resolution
- Conduct thorough literature and data research to address complex customer medical inquiries across oncology, neurology, and immunology product lines
- Evaluate scientific and medical literature to support evidence-based content development
- Provide country and regional medical information support in alignment with global standards and regulatory requirements
- Execute departmental processes and contribute to cross-functional projects in collaboration with MI&I colleagues across global business units
- Generate reports and analyze data to identify trends, insights, and opportunities for content improvement
- Participate in stakeholder meetings and contribute meaningfully to strategic discussions and content initiatives
- Support medical information activities across multiple products, including oncology and neurology therapies
- Maintain and manage content within medical information databases and file management systems
- Attend and travel to medical conferences as required, approximately one 3-day conference annually
- Exceptional medical writing skills with the ability to develop multi-level, audience-appropriate scientific responses
- Strong scientific literature evaluation and critical appraisal capabilities
- Mastery of the English language, both written and spoken, with outstanding oral and written communication skills
- Excellent interpersonal and presentation skills with the ability to engage confidently with internal and external stakeholders
- Proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint
- Experience with medical information content and inquiry management systems, including Veeva Vault and Salesforce
- Familiarity with scientific literature research tools and databases
- Ability to generate and interpret reports and derive actionable insights from data analysis
- Experience utilizing AI tools to enhance productivity and content quality is a plus
- Self-driven, independent thinker capable of working with limited oversight and contributing innovative ideas
- Strong organizational and file management skills with high attention to detail
- Minimum of a Master's degree or higher in a scientific field such as biology or a related discipline required
- Doctorate degree from an accredited college or university (e.g., M.D., Ph.D., PharmD, or equivalent) preferred
- Minimum of 3 years of medical writing experience required in the pharmaceutical industry, a clinical setting, or equivalent background preferred
- Experience supporting medical information activities across specialty care therapeutic areas, particularly oncology and/or neurology
- Demonstrated experience developing scientific response letters and managing medical information content
Salary : $64