Under departmental supervision, the Associate Medical Writer will prepare simple clinical documents.
Perform edits and format changes on documents, as requested. Assist with final quality control check, compilation, formatting, tabulation, and pagination of documents.
Prepare documents such as patient narratives, upfront/shell reports and complete study reports, under the supervision of the project lead Medical Writer.
Excellent interpersonal, verbal and written communication skills.
Client focused approach to work.
A flexible attitude with respect to work assignments and new learning.

The Associate Medical Writer must be conscientious, able to work with minimal supervision, have an aptitude for working with a variety of different software packages, exhibit a high degree of flexibility and initiative, demonstrate the ability to follow up on multiple tasks and projects, and possess the ability to handle matters of a confidential nature.

Qualifications

Graduate or Postgraduate in Life Sciences. Scientific background essential. Some experience of medical writing of regulatory documents such as patient narratives, informed consent forms or similar in a contract research organization, pharmaceutical or biotechnology firm, or some experience in the conduct of clinical research/medical communications.

 

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