Senior Regulatory Medical Writer III — Hybrid, Global Trials
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Johnson & Johnson Innovative Medicine seeks a Medical Writer III, Regulatory Medical Writing to support across key therapeutic areas within IDAR. The role may be in Maidenhead, Leiden, Neuss, Paris, or Beerse and follows a hybrid model with three onsite days weekly.
Responsibilities include writing or coordinating regulatory documents (CSRs, IBs, protocols, summaries); leading cross-functional document planning; mentoring junior writers; and driving process improvements.
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Senior Regulatory Medical Writer III — Hybrid, Global Trials
Il y a 2 heures
Antwerp, Flanders, Belgique Johnson & Johnson Innovative Medicine Temps pleinpJohnson Johnson Innovative Medicine seeks a Medical Writer III, Regulatory Medical Writing to support across key therapeutic areas within IDAR. The role may be in Maidenhead, Leiden, Neuss, Paris, or Beerse and follows a hybrid model with three onsite days weekly. /ppResponsibilities include writing or coordinating regulatory documents (CSRs, IBs,...
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Senior Regulatory Medical Writer III — Hybrid, Global Trials
Il y a 3 heures
Antwerp, Flanders, Belgique Johnson & Johnson Innovative Medicine Temps pleinJohnson & Johnson Innovative Medicine seeks a Medical Writer III, Regulatory Medical Writing to support across key therapeutic areas within IDAR. The role may be in Maidenhead, Leiden, Neuss, Paris, or Beerse and follows a hybrid model with three onsite days weekly. Responsibilities include writing or coordinating regulatory documents (CSRs, IBs, protocols,...
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Beerse, Antwerp, Belgium, VLG Johnson Johnson Télétravail Temps plein 79 800 € - 137 770 € ContratAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to...