Medical Writer - Publications

Responsibilities:

Generate documents for various stages of drug development, such as manuscripts, abstracts, posters, oral presentations, and slide sets, overseeing their entire life cycle.
Independently draft initial versions based on study reports and/or source data, encompassing primary and secondary analyses, with input from the lead author.
Manage or complete submissions to journals and conferences, ensuring compliance with their respective requirements.
Undertake Project Management duties, including formulating and adhering to timelines, leading kick-off meetings, scheduling and overseeing gatherings, while showcasing strong interpersonal, negotiation, and flexibility skills.
Offer professional guidance to authoring teams to ensure adherence to GPP 2022, ICMJE guidelines, and other industry standards and best practices.
Oversee document reviews, address comments, and facilitate discussions on comment resolution with internal and external authors.
Secure and maintain necessary documentation for publication in accordance with client policies.
Comprehend and adhere to all client publication policies and procedures, encompassing confidentiality, secure file transfer, copyright law, and privacy protection.

Qualifications:

Education, Experience, Training, and Knowledge:

PhD, MD, MPH, or PharmD required, or equivalent experience.
A minimum of 7+ years of experience as a professional medical writer, contributing to or creating numerous medical publications, manuscripts, presentations, and posters.
Advanced graphic skills to produce high-quality publication figures.
Experience in developing manuscript enhancements and extenders.
Preferred experience in grant proposal writing and supporting advisory boards.
Preferred experience in medical information and educational materials.