Senior Regulatory Medical Writer: Submissions Lead

Senior Regulatory Medical Writer: Submissions Lead

Full-Time 40000 - 50000 Β£ / year (est.) No working from home possible
Meeveem Limited

At a Glance

  • Tasks: Lead the creation of regulatory documents and coordinate activities across departments.
  • Company: Join Syneos Health, a leader in the healthcare industry.
  • Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
  • Other info: Mentor junior writers and thrive in a dynamic, collaborative environment.
  • Why this job: Make a significant impact on healthcare by delivering high-quality submissions.
  • Qualifications: Experience in medical writing and strong communication skills required.

The predicted salary is between 40000 - 50000 Β£ per year.

Syneos Health is seeking an experienced Medical Writer to lead the creation of regulatory and scientific documents for multiple studies.

You will coordinate activities across departments, respond to client comments, and ensure all materials meet ICH guidelines and internal SOPs.

The role involves mentoring junior writers, reviewing statistical plans, and maintaining timelines and budgets while delivering high-quality manuscripts and submissions for meetings and regulatory filings.

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Senior Regulatory Medical Writer: Submissions Lead employer: Meeveem Limited

Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.

Meeveem Limited

Contact Details:

Meeveem Limited Recruitment Team

We think you need these skills to ace Senior Regulatory Medical Writer: Submissions Lead

Regulatory Writing
Scientific Document Creation
ICH Guidelines
SOP Compliance
Mentoring
Statistical Plan Review
Project Coordination