As a Sr. Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
Develop regulatory documents for submission to regulatory agencies globally, in accordance with ICH and other global guidelines, standards and processes, and AMA Medical Writing styles, as applicable, in adherence with study/project timelines and corporate objectives.
· Actively participate in study and/or project team meetings to provide input regarding medical writing deliverables, timelines and any processes needed for the completion of regulatory documents.
· Administrate as appropriate, the receipt, collation, and incorporation of review comments needed for the completion of regulatory documents.
· Review other documents associated with the assigned project(s) (eg, Protocols and Statistical Analysis Plans), as appropriate.
· Assist in defining and writing standard operating procedures and working practices to allow the effective and efficient preparation of quality documents.
· May participate in cross-functional process improvement initiatives.
You are:
A Bachelor's degree in life science discipline with Master's degree in life science discipline preferred.
· At least 5 years of medical writing experience in the biopharmaceutical/CRO industry required or comparable experience within clinical or preclinical development.
· Understanding and knowledge of global regulatory requirements.
· Knowledge of the various phases of clinical development required.
· Proficiency in organizing and communicating clinical information required.
· Strong communication, organizational, time management, and project management skills are required.
· Strong verbal, written, and interpersonal communication skills needed to work effectively in a team environment.
· Proficient in MS Word.
· Experience with an electronic document management system (eg, Documentum, Master Control) and templates is preferred.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
https://careers.iconplc.com/reasonable-accommodations
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
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