Medical Writer III, Regulatory Medical Writing, X-TA - Issy-les-Moulineaux
il y a 1 mois
Job summary
We are searching for the best talent for a Medical Writer III to support across key therapeutic areas within our Integrated Data Analytics & Reporting business.The position may be located High Wycombe UK 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.
You will be responsible for writing or coordinating clinical and regulatory documents such as CSRs IBs protocols summary documents RMPs regulatory responses and briefing documents leading cross-functional document planning and review meetings interacting with cross-functional colleagues on document content acting as a champion of medical writing processes using your experience in scientific discipline at least six years pharmaceutical/scientific relevant experience four years medical writing required excellent oral written communication skills pivotal to engage in discussions English fluency required attention to detail able function team environment strong project/time management leadership skills resolve problems under supervision demonstrate learning agility build solid productive relationships with cross-functional team members.
Description du poste
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