Regulatory Document Specialist

2 days ago


West Berkshire, United Kingdom Proclinical Staffing Full time
Job Description

As a Senior Manager, Medical Writing, you will be responsible for leading a team of writers to create and maintain clinical documents. This role requires strong leadership and communication skills, as well as the ability to prioritize tasks effectively and manage multiple projects simultaneously.

Key Responsibilities:

  • Develop and implement a content strategy that aligns with company goals.
  • Collaborate with cross-functional teams to ensure seamless project execution.
  • Develop and maintain SOPs and templates to support efficient document production.
  • Maintain knowledge of industry regulations and guidelines to ensure compliance.

Requirements:

  • Bachelor's degree in Life Science or English/Communications with relevant expertise.
  • Minimum 5 years of experience in medical writing, preferably with regulatory submissions.
  • Strong leadership and communication skills to motivate and guide team members.
  • Estimated salary: $120,000 - $150,000 per annum, depending on experience.

Benefits:

  • Health insurance and retirement plan.
  • Paid time off and flexible working hours.


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