Organizational Overview:

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 Director, Medical Writing Operations & Regulatory Business Operations, this position is responsible for partnering cross-functionally to deliver high quality regulatory and clinical documents.

Key Responsibilities: 

• Coordinate and author clinical and regulatory documents to ensure integration of scientific and medical input from development team members.

• Lead submission-level documents at the project manager level and handle all components of writing clinical regulatory documents (e.g., Protocols, clinical study reports [CSRs], investigator brochures [IBs], etc.,).

• Contribute to strategy from a medical writing perspective.

• Assure documents are in accordance with the International Council for Harmonisation (ICH) and other regulatory guidelines.

• Represent medical writing at cross-functional meetings (e.g., kick-off meetings [KOMs], comment resolution meetings, strategy discussions, etc.,) and provide information regarding requirements for medical writing deliverables.

• Review protocols; amendments; statistical analysis plans (SAPs); table shells; tables, listings, and figures (TLFs), regulatory responses, and other regulatory documents to ensure consistency across all documents.

• Raise any concerns regarding inconsistencies across documents or writers with the IMVT Director or Medical Writing to resolve and ensure consistency across both assets.

• Arrange and lead team review meetings over the course of project progression.

• Produce high-quality and timely documentation and provide input on data analysis, planning, and interpretation.

• Maintain strict timelines as project lead.

• Coordinate QC review of documents.

• Mentor junior writers that are within the team.

Requirements:

• S./B.A. degree required, advanced degree highly desirable

• Minimum of 5 years of relevant medical writing experience in the pharmaceutical industry, especially writing in one or more of the ophthalmology or rare diseases therapeutic areas.

• An understanding of the drug development process.

• Experience in interacting with cross functional study team members Knowledge, Skills, and Abilities:

o Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research and medical writing standards; demonstrated ability to interpret and apply these guidelines to document writing.

o Ability to work independently with minimal supervision, multi-task, and work effectively under pressure; adapt to change as needed; possess excellent project management skills; attentive to details.

o Ability to communicate with teams to set realistic timeline expectations; demonstrated ability to deliver within agreed internal and regulatory timelines; monitor and communicate progress against milestones; escalate complex issues appropriately.

o Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with team members.

o Ability to utilize a balanced approach to problems, using flexibility and persistence as appropriate.

o Read, write, and speak fluent English; excellent verbal and written communication skills.

Work Environment:

• Remote-based

• Dynamic, interactive, fast-paced, and entrepreneurial environment

• Domestic or international travel are required (10-20%)

Salary and compensation

No salary data published by company so we estimated salary based on similar jobs related to Non Tech and Non Tech jobs that are similar:

$30,000 — $50,000/year