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Medical Writer

Medical Writer

Your new company
Top Global pharmaceutical

Your new role
To accomplish their primary goal of communicating complex medical information in clear and compliant writing. Work with clinical teams and clients to understand the nature of the scientific work that they will be covering. Assess data or products using medical expertise, and quickly develop expertise in new areas as needed for their writing. Conduct comprehensive literature searches to enhance background understanding, and evaluate and analyze the information.

What you'll need to succeed
Responsibilities Compile, write, and edit medical writing deliverables covering all phases of clinical research for submission to regulatory agencies. Writings include but not limited to comprehensive clinical study reports, study protocols, annual reports, investigator brochures, risk/benefit analysis and integrated summaries from raw data. The writing is also used in publications or medical journals, or for internal company use. Also write scientific copy for a broader audience, including scientific liaisons, healthcare professionals, and pharmaceutical representatives. Prepare abstracts, scientific exhibits, posters and verbal presentations. Develop and write pharmaceutical training materials, eLearning content, video scripts, magazine articles, and presentations to be used by a variety of audiences. A key task is to be sure that all deliverables are in accordance with regulations, standards, and guidelines. The regulatory documents must meet ICH, GLPs, and GCPs guidelines, a writing style guide, and often the company template. Must understand the levels of evidence required to achieve regulatory, marketing and regulatory goals.

What you'll get in return

Master degree is required. Extensive knowledge of English grammar with a familiarity with a standard style guide. Ability to communicate scientific or medical information in a clear and concise manner. Proficiency in Word, Excel, PowerPoint, email, and the Internet. Familiarity with the principles of clinical research. Ability to interpret and present clinical data and other complex information. Be aware of current industry practices and regulatory requirements that affect medical writing. Keep abreast of current literature, emerging science, technological developments and medical trends.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.

Summary

Job type:
Permanent
Working Pattern
Full-time
Industry
Pharmaceuticals
Location
China
Specialism
Medical Affairs
Pay
£50000-£80000
Ref:
3654928
Apply Now

Talk to a consultant

Talk to Sudan Peng, the specialist consultant managing this position, located in London City

4th Floor, 107 Cheapside

Telephone: 02034650158

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