Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases.
The Role:
Reporting to the Senior Director, Medical Communications, this position is responsible for developing scientific content across medical communication activities.
Key Responsibilities:
Develop global medical materials, including publications, FAQs, MSL training materials, congress booth materials, etc
Develop high-quality scientific publications, including abstracts, posters, outlines, primary and review articles, supplements, monographs, slide presentations, meeting summaries, and other materials
Develop manuscripts that meet the stated objectives of the project, are within the job specifications as defined by team, are at the appropriate level and tone for the audience, and adhere to good publication practices
Review and proofread materials to check quality and scientific accuracy and to ensure that the content, format, and structure of their documents comply with regulatory, journal, or other guidelines
Monitor deadlines and ensure projects are delivered on time to align with other company-wide projects
Liaise directly with KOLs and authors/speakers on various projects and participate in on-site review before any virtual or live event
Manage external writers supporting assigned projects, as needed
Partner with the medical and clinical development team to develop congress materials as it relates to presentations and booth materials.
Support medical communications planning in collaboration with the Medical Communications Lead
Requirements:
Advanced degree (PharmD, M.D. or Ph.D.) preferred but not required
5+ years of medical writing experience
Experience in medical publications required, including abstracts, posters, oral presentations and manuscripts
Experience developing field medical and congress booth materials preferred
Knowledge of current requirements and guidelines applicable to medical affairs/medical communications documents e.g., GPP, ICJME.
A superb command of the English language, both written and spoken; faultless grammar and spelling
Demonstrated ability to work with a diverse set of stakeholders on
multiple projects
Work Environment:
Remote-based
Dynamic, interactive, fast-paced, and entrepreneurial environment
Domestic or international travel are required (5-15%)
Compensation is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. Equity, sign-on bonuses, and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, dental, vision, 401k and other benefits, including unlimited paid time off and parental leave.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Writing/Editing and Science
Industries
Biotechnology Research and Pharmaceutical Manufacturing
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