Senior Medical Information Writer

At EVERSANA, we are proud to be certified as a Great Place to Work across the globe. We’re fueled by our vision to create a healthier world. How? Our global team of more than 7,000 employees is committed to creating and delivering next-generation commercialization services to the life sciences industry. We are grounded in our cultural beliefs and serve more than 650 clients ranging from innovative biotech start-ups to established pharmaceutical companies. Our products, services and solutions help bring innovative therapies to market and support the patients who depend on them. Our jobs, skills and talents are unique, but together we make an impact every day. Join us! Across our growing organization, we embrace diversity in backgrounds and experiences. Improving patient lives around the world is a priority, and we need people from all backgrounds and swaths of life to help build the future of the healthcare and the life sciences industry. We believe our people make all the difference in cultivating an inclusive culture that embraces our cultural beliefs.  We are deliberate and self-reflective about the kind of team and culture we are building. We look for team members that are not only strong in their own aptitudes but also who care deeply about EVERSANA, our people, clients and most importantly, the patients we serve.   We are EVERSANA.  THE POSITION: At EVERSANA, our integrated life sciences compliance team is taking a leading role in helping some of the most scientifically advanced Biopharma and research companies around the world to innovate novel therapies for rare, ultra-rare and a range of critical therapeutic areas including Oncology, Neurology, Immuno-oncology, Immunology, etc. This role is within the EVERSANA Compliance team, reporting directly to the Director, Medical Content Development and Medical Review. This person will also collaborate very closely with other team members within the EVERSANA Compliance Business Unit (Medical Information (MI), and Medical Affairs). This position will support various types of clients including pharmaceutical, biotechnology, medical devices, digital therapeutics, and over-the-counter companies. This position is responsible for MI content development-related client engagements. ESSENTIAL DUTIES AND RESPONSIBILITIES: Our employees are tasked with delivering excellent business results through the efforts of their teams.  These results are achieved by:   Develop, review, and maintain scientifically accurate, evidence-based Medical Information (MI) content, including Scientific Response Documents (SRDs), Global Response Documents (GRDs), Customized Response Documents (CRDs), FAQs, cover letters, training materials, and other medical information and scientific communication resources. Independently manage the end-to-end MI content development lifecycle, including literature searches, synthesis of evidence, content authoring, incorporation of stakeholder feedback, document finalization, and coordination of Medical, Legal, and Regulatory (MLR) review processes. Serve as the primary content owner within document management systems (Veeva Vault Systems), ensuring accurate document upload, lifecycle management, version control, reference linking, annotation, and compliance with documentation standards and regulatory requirements. Conduct quality control and peer reviews, scientific data verification, and reference validation to ensure accuracy, consistency, scientific rigor, and compliance of MI deliverables. Manage translation requests and coordinate with external translation vendors to ensure timely delivery of high-quality, scientifically accurate, and locally compliant medical information materials. Participate in client-facing and internal meetings to provide scientific expertise, project updates, and recommendations on MI content and communication strategies. Support the development, review, and continuous enhancement of Standard Operating Procedures (SOPs), work instructions, templates, style guides, quality checklists, and process documentation to drive operational excellence and compliance. Ensure all medical information materials are scientifically balanced, evidence-based, compliant with applicable regulatory and company requirements, and aligned with industry best practices. Responsible for proactively flagging and managing any quality issues, and ensure timely corrective and preventive actions Stays knowledgeable of industry best practices and supports leadership team in evaluating and implementing new technologies and procedures to improve operational efficiency and quality of materials developed. Works collaboratively with other medical writers and creative teams across EVERSANA. Demonstrate a commitment to diversity, equity, and inclusion through continuous development, modeling inclusive behaviors, and proactively managing bias. All other duties as assigned. EXPECTATIONS OF THE JOB: Responsible for delivering CLIENT DELIGHT Responsible for working collaboratively with EVERSANA medical information and medical affairs team and taking directions and feedback from management and clients Responsible for ensuring management and compliance with industry standards and codes of practice Able to work independently to develop high-quality, scientifically accurate, strategically aligned, ethical, and compliant medical content Responsible to proactively flag and manage any quality issues, and ensure timely corrective and preventive actions Hours : Able to work full time and be flexible with work scheduling as required by clients and management. (40+ hours per week, 5 days of the week) MINIMUM KNOWLEDGE, SKILLS AND ABILITIES: The requirements listed below are representative of the experience, education, knowledge, skill and/or abilities required.   Education: Minimum bachelor’s degree in scientific discipline or healthcare; Master’s, PhD, or PharmD preferred Experience: Minimum of 2 years of MI writing and medical content development experience Exceptional communication skills include written, oral, interpersonal, and presentation skills including the ability to independently interpret and summarize complex results. Ability to effectively interface with all levels of management and staff and to succeed in a matrix team setting while meetings or exceeding timelines. Familiarity with AMA Style guide as well as an understanding of clinical research principles and applied statistics. Familiarity with International Committee of Medical Journal Editors (ICMJE), Good Publication Practices (GPP), and other medical publishing guidelines (e.g., Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), Strengthening the Reporting of Observational Studies in Epidemiology (STROBE), Consolidated Standards of Reporting Trials (CONSORT), etc. Proficient editing skills along with expertise in Microsoft Office, Acrobat and other applications. Experience conducting literature searches and working with tools such as PubMed, Ovid, Embase, etc. Experience working with reference management and citation software (e.g., EndNote, Mendeley, Citavi, etc.) Strong understanding of regulatory requirements and best practices in relationship to Medical Information, Medical Affairs and promotional and non-promotional materials review. Excellent project management skills and proven track record of being results driven; ability to manage Ability to conceptualize, design and deliver best in class solutions Highly pri