Medical Writer II Home Based

ICON - Be a Part of our Journey...

Are you interested in improving your knowledge of Clinical Trials and contributing to our culture of process improvement with a focus on streamlining our processes of adding value to our business and meeting client needs?

Medical Writer ll  role within ICON HOME BASED:

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.

The successful candidate will review and interpret clinical data; to independently write, edit, review, QC and compile documents (largely protocols and clinical study reports) from phase 1/2a studies, with an emphasis on healthy volunteer, clinical pharmacology studies, and some early patient studies, in a CRO setting for multiple clients; to manage medical writing tasks; to ensure the accuracy and quality of applicable written deliverables; and compliance with ethical, legal, regulatory and client standards. 

We are presently in over 40 countries with over 80 offices worldwide and over 12K employees globally.  We are comprised of 6 divisions and offer a full-service portfolio of solutions to our clients. 

Benefits of working at ICON:

We provide a Medical Writer ll with the resources to be successful and introduction to the study start up field with career progression toward all aspects of distributing regulatory documents for participating investigator sites. In addition, we offer excellent health, dental, vision and life insurance coverage; 401(K) with company match; competitive pay; generous time off; and bonus incentives

To succeed you will need:

·         Bachelor’s Degree in biological or related sciences with a minimum of 2 years regulatory medical writing experience.  CRO experience preferred.

·         Must have experience authoring Phase 1 clinical protocols and clinical study reports

·         Must possess excellent grammatical, editorial and proofreading skills and have the ability to interpret and present complex data

·         Must have a solid understanding of FDA/ICH guidelines and GCPs.

·         Proficiency in use of Microsoft Word, Excel, and PowerPoint