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.
Job Description
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 principled – proves to be a professional of unquestionable integrity, credibility and character who demonstrates high moral and ethical behavior
Collaboration – Ability to work cross functionally across EVERSANA business units and with various clients, including leadership and various departments and functions of our clients
Agile learning – Ability to support and learn about multiple disease states and therapeutic areas
Qualifications
Education: PharmD (or M. Pharm or M.S. Pharm), PhD, or MD
Experience: Strong expertise in MI content development and scientific writing, with a track record of delivering accurate, evidence-based, and compliant medical communications.
Broad therapeutic area experience with the ability to effectively manage diverse product portfolios and complex scientific content.
Proficiency in Veeva Vault System, including document management, workflow administration, content promotion processes, and MLR review support.
Additional Information
All your information will be kept confidential according to EEO guidelines.
Our team is aware of recent fraudulent job offers in the market, misrepresenting EVERSANA. Recruitment fraud is a sophisticated scam commonly perpetrated through online services using fake websites, unsolicited e-mails, or even text messages claiming to be a legitimate company. Some of these scams request personal information and even payment for training or job application fees. Please know EVERSANA would never require personal information nor payment of any kind during the employment process. We respect the personal rights of all candidates looking to explore careers at EVERSANA.
From EVERSANA’s inception, Diversity, Equity & Inclusion have always been key to our success. We are an Equal Opportunity Employer, and our employees are people with different strengths, experiences, and backgrounds who share a passion for im

Work arrangement
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