Medical Writer III, X-TA

h3Job Function: /h3 pMedical Affairs Group /p h3Job Sub Function: /h3 pMedical Writing /p h3Job Category: /h3 pProfessional /p h3All Job Posting Locations: /h3 pIssy-les-Moulineaux, France, Leiden, South Holland, Netherlands, Neuss, North Rhine-Westphalia, Germany, Turnhout, Antwerp, Belgium /p h3Job Description /h3 h3About Innovative Medicine /h3 pOur 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. /p pJoin us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. /p pLearn more at /p pWe are searching for the best talent for a bMedical Writer III, Regulatory Medical Writing /bto support across key therapeutic areas (X-TA) within our Integrated Data Analytics Reporting (IDAR) business. The position may be located bMaidenhead, UK; Leiden, Netherlands; Neuss, Germany; Paris, France; or Beerse, Belgium. /b /p pThe 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. /p pPlease 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): /p pUnited Kingdom -Requisition Number: R
- /p pBelgium/Netherlands/France/Germany
- Requisition Number: R
- /p pRemember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission. /p pAre you ready to join our team? Then please read further /p h3You Will Be Responsible For: /h3 ul liWriting or coordinating clinical and regulatory documents such as, but not limited to, CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents. /li liLeading 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. /li liWill 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). /li liCoach or mentor of more junior staff on document planning, processes, and content. Provides peer review as needed. /li liActive participant in or lead of process working groups. /li /ul h3Qualifications /

Requirements:
/h3 ul liA university/college degree in a scientific discipline is required. An advanced degree (eg, Masters, PhD, MD) preferred. /li liAt least 6 years of relevant pharmaceutical/scientific; at least 4 years of relevant medical writing experience is required. /li liExcellent oral and written communication skills are pivotal to engage in cross-functional discussions. /li liEnglish fluency required. /li liAttention to detail. /li liAble to function in a team environment. /li liStrong project/time management skills. /li liStrong project/process leadership skills. /li liAble to resolve complex problems under supervision. /li liDemonstrate learning agility. /liliAble to build solid and productive relationships with cross-functional team members. /li /ul h3Benefits /h3 pWe 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 organisation. For additional general information on company benefits, please go to: /p pJohnson Johnson is an Affined Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit /p ul liThe Netherlands: The anticipated base pay range for this position is 64,000
- 103,040 Euro. /li liBelgium: The anticipated base pay range for this position is 72,500
- 115,230 Euro. /li liFrance: The anticipated base pay range for this position is 53,500
- 85,790 Euro. /li liGermany: The anticipated base pay range for this position is 75,000
- 118,450 Euro. /li /ul pIn addition to base pay,

we offer
the following benefits*: an annual bonus wit