Oncology Regulatory Content Lead

2 weeks ago


Espoo, Uusimaa, Finland Johnson & Johnson Full time
About the Role:

We are seeking an experienced Oncology Regulatory Content Lead to join our team at Johnson & Johnson. The successful candidate will be responsible for developing and implementing content strategies to support our oncology products.

Key Responsibilities:
  • Develop and maintain high-quality content to support regulatory submissions.
  • Collaborate with cross-functional teams to ensure that our content meets the highest standards of safety and efficacy.
  • Provide guidance and training to junior staff members on content planning, processes, and best practices.
  • Actively participate in content and cross-functional meetings.
  • Maintain knowledge of industry, company, and regulatory guidelines.

Requirements:
  • At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience is required.
  • Oncology therapeutic area experience preferred.
  • Excellent oral and written communication skills are pivotal to engage in cross-functional discussions.
  • Expert project/time management skills.
  • Able to recognize how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content.


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