Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as Associate Medical Writer – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our expert team, you’ll have the prospect to ensure operational excellence that makes a real difference in organizational performance. As Associate Medical Writer, you will assist with the preparation of high-quality medical and scientific writing from planning and coordination through the delivery of final drafts to internal and external clients. You will collaborate with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.
What You’ll Do:
• Assists with researching, writing, and editing routine documents including Informed consent forms, Lay summaries, and other patient centric documents.
• May assist with more complex clinical and scientific and program level documents.
• Assists with ensuring compliance with quality processes and requirements for assigned documents.
• May assist in program management activities. Duties could include assisting with developing timelines, budgets, and forecasts.
• Participates in project launch meetings, review meetings, and project team meetings.
Education and Experience Requirements:
• Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 to 3 years).
• Experience working in the pharmaceutical/CRO industry advantageous
• Experience in scientific writing advantageous
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual