Regulatory Document Writer

5 giorni fa


Roma, Lazio, Italia MMS Holdings Inc. A tempo pieno

MMS Holdings Inc. is a leading provider of clinical data solutions for the pharmaceutical industry. As a Senior Medical Writing Consultant, you will play a crucial role in our team, helping to deliver high-quality clinical documents to our clients.

Key Responsibilities:

  • Develop and maintain a deep understanding of regulatory requirements and industry standards for clinical document writing.
  • Write and edit clinical development documents, including protocols, investigator brochures, study reports, and other regulatory documents.
  • Collaborate with cross-functional teams to ensure that documents meet client needs and regulatory requirements.
  • Maintain strong relationships with clients and internal stakeholders to ensure timely delivery of high-quality documents.

Requirements:

  • 3+ years of experience in regulatory writing and clinical document authoring.
  • Proven track record of delivering high-quality documents on time and on budget.
  • Strong understanding of regulatory requirements and industry standards.
  • Excellent writing, editing, and communication skills.

MMS Holdings Inc. offers a dynamic and supportive work environment, competitive compensation, and opportunities for professional growth and development.


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