Medical Writer III, X-TA

Job Function: Medical Affairs Group Job Sub Function: Medical Writing Job Category: Professional All Job Posting Locations: High Wycombe, Buckinghamshire, United Kingdom Job Description: About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at innovative-medicine We are searching for the best talent for a Medical Writer III, Regulatory Medical Writing to support across key therapeutic areas (X-TA) within our Integrated Data Analytics Leiden, Netherlands; Neuss, Germany; Paris, France; or Beerse, Belgium. The position is Hybrid (3 days onsite weekly). Remote work options may be considered on a case‑by‑case basis and if approved by the company. Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s): United Kingdom -Requisition Number: R-103733 Belgium/Netherlands/France/Germany -Requisition Number: R-104917 You will be responsible for: Writing or coordinating clinical and regulatory documents such as, but not limited to, CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents. Leading cross‑functional (eg, with clinical team) document planning and review meetings. Interacting with cross‑functional colleagues on document content and acting as a champion of medical writing processes and best practices. Responsible for establishing document timelines and strategies in accordance with internal processes, with some mentorship from functional management and clinical team, as needed. Will function as a lead writer on most compounds (or submissions, indications, or disease areas) under supervision. Will be primary point of contact for medical writing activities for the cross‑functional team (eg, clinical). Coach or mentor of more junior staff on document planning, processes, and content. Provides peer review as needed. Active participant in or lead of process working groups. Qualifications / Requirements: A university/college degree in a scientific discipline is required. An advanced degree (eg, Masters, PhD, MD) preferred. At least 6 years of relevant pharmaceutical/scientific; at least 4 years of relevant medical writing experience is required. Excellent oral and written communication skills are pivotal to engage in cross‑functional discussions. English fluency required. Attention to detail. Able to function in a team environment. Strong project/time management skills. Strong project/process leadership skills. Able to resolve complex problems under supervision. Demonstrate learning agility. Able to build solid and productive relationships with cross‑functional team members. Benefits We offer a competitive salary and extensive benefits package. The health and well‑being of our employees is a priority, we have a flexible working environment as we value work‑life balance. We offer career development opportunities for those who want to grow and be part of our organization. Equal Opportunity Employer Johnson