Senior Medical Writer

Planet Pharma is working with a global CRO seeking a Senior Medical Writer to join on a 12-month contract.

As a Senior Medical Writer, you will be responsible for preparing critical clinical and regulatory documents, including:

• Protocols
• Investigator Brochures (IBs)
• Informed Consent Forms (ICFs)
• Clinical Evaluation Reports (CERs)
• Regulatory Submissions

Your expertise will ensure timely, clear, and accurate communication across teams and stakeholders.

Key Responsibilities

• Author critical documents, including protocols, IBs, ICFs, CERs, PIPs, and regulatory submissions
• Lead clinical writing discussions, ensuring strategy alignment and stakeholder engagement
• Interpret and summarize clinical data for regulatory approval
• Provide guidance and training to other writers
• Manage multiple assignments, prioritizing efficiently
• Ensure compliance with Fortrea and client SOPs

Required Skills

• Strong communication and leadership in cross-functional teams
• Project management expertise, driving tasks to completion
• Ability to work independently, solving challenges proactively
• Experience as a lead writer on submission documents

If you would like to discuss this vacancy further or explore your career options in confidence, please email us.

We are an equal opportunities recruitment business and agency, welcoming applications from all qualified candidates regardless of race, sex, disability, religion/belief, sexual orientation, or age. Planet Pharma provides global staffing services.