Fsp Medical Writer

PPD (Thermo Fisher) UK

Bangalore, India
Clinical and regulatory document writing
Collaboration with cross-functional teams
Regulatory guidelines compliance
At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale

Job Summary

  • At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale.
  • The Medical Writer will be responsible for developing high-quality clinical and regulatory documents, ensuring they meet all regulatory requirements and company standards.
  • PPD clinical research services offers a collaborative environment with a flexible working culture and an extensive benefits package focused on employee health and well-being.

Matching Summary

At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale.

Skills & Requirements

Must-have

  • Clinical and regulatory document writing
  • Collaboration with cross-functional teams
  • Regulatory guidelines compliance
  • Document quality control
  • Project timeline management

Nice-to-have

  • Structured content authoring systems
  • AI-driven content creation
  • Leadership and mentoring skills
  • Flexible working culture
  • Award-winning learning and development

Key Requirements

  • Bachelor's degree in scientific discipline
  • 2+ years regulatory writing experience
  • Experience in pharmaceutical/CRO industry
  • Knowledge of regulatory guidelines
  • Safety writing experience advantageous

Work Rights

Not specified

Tailored Resume

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