The position of Medical Writer in IQVIA will help you elevate your career in the CRO industry.
Essential Functions :
Preparing assigned documents, confirming templates and specifications, negotiating and adhering to timelines.
Organizing document reviews, communicating directly with the customer.
Planning and organizing workload for assigned projects and tasks : identify project needs, track timelines and implement customer requests.
May lead meetings on more challenging topics independently.
Degree in life sciences
Typically requires at least 3 years of highly relevant experience.
In-depth knowledge of the structural and content requirements of clinical study reports, protocols, and similar documents and ability to identify deficiencies, errors, and inconsistencies in a protocol or report.
Good understanding of common statistical methods used in clinical trials and / or interpretation of their results .
Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
Significant experience in preparing CSRs and protocols .
In depth knowledge of drug development, medical writing, and associated regulations.
Excellent written and oral communication skills including grammatical / technical writing skills.
Excellent attention to detail and accuracy.
If you think you are able to bring to the role ability to adapt rapidly changing environment, problem solving attitude and constant readiness to upgrade, please apply.
LI - MS8