Senior Medical Writer

Why you want to join:

• A world class innovative business 
• Opportunity to work on projects for global pharmaceutical and biotech companies working on cutting edge drug discovery
• Further develop your medical writing skills
• Mix of home and office based working

As part of a close knit team, who work to the highest standards, you will manage a varied work load covering all documents from investigator brochures, clinical study protocols, clinical study reports through to summary documents as well as articles.

Key Responsibilities

• Preparing and writing clinical study documents including regulatory documents
• Quality control and review
• Project management of multiple documents and assignments
• Assist with departmental projects
• Liaising directly with clients

Requirements

• Life Sciences degree  
• Previous medical writing experience in a CRO environment
• Strong experience in writing and editing clinical regulatory documents
• Great understanding of medical/regulatory local and national regulations
• Excellent knowledge of Microsoft Office
• Proactive with great time management and communication skills
• Ability to work collaboratively and in a fast paced and busy environment

Park Street People Ltd does not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and complies with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.