Role of Medical Writer in Clinical Research

The success of Medical writing in clinical research depends upon the proper documentation and the exactness of the research, its planning and results. Cognibrain’s medical writers are experienced in a broad range of therapeutic areas and can assist you at any point in your content development life-cycle

Role of a Medical Writer In Clinical Research:

• Clinical trials are important For The new drugs to come into the Market
• Conducting A Clinical Trial Is Not the end Of Clinical Research
• Research Data Has to Be Presented In Clear Concise Manner

Who does this job?

• Research Scientists
• Doctors
• Statisticians
• Regulatory professionals
• Medical writer

What does a medical writer do?

Prepares scientific documents of highest quality meeting all applicable regulatory requirements.

Industries requiring medical writing services:

• Pharmaceutical Industry
• Clinical Research
• Pharmacovigilance
• Healthcare

Documents prepared by medical writer:

• Research proposals
• Investigator brochures
• Informed consent documents
• Clinical study reports
• Clinical trial protocols
• Package inserts
• Patient information leaflets
• Patient safety narratives

Who is the best medical writer for you?

• Has knowledge of drug development process
• Has knowledge of regulatory requirements like FDA, EMEA etc.
• Understands the purpose and requirement of the task
• Can logically organize thoughts and ideas
• Has good coordination with stakeholders or team

What else to look for?

• Training in AMA writing style
• Experience in publication related standards
• Ethics in conduct and reporting of research

Medical Writing Company Offers:

• Zealous medical writers across all therapeutic areas
• Medical writers trained in AMA style of writing
• Medical writers experienced in publication standards and regulatory requirements
• Regulatory and Pharmacovigilance medical writing