MJH Life Sciences®

The Principal Medical Writer will lead the development of high-quality scientific content across various therapeutic areas and ensure compliance with industry standards. Responsibilities include conducting literature reviews, managing writers, and preparing materials for promotional review processes.

The Scientific Director owns the scientific vision for oncology education programs, translating complex clinical data into content for live events and videos. They lead scientific strategy across multiple accounts, manage client relationships, and mentor medical writing staff.

You will build and maintain web applications, APIs, and AI-powered workflows while owning the full development lifecycle from problem definition to deployment. The role involves collaborating with stakeholders to integrate enterprise systems and optimize cloud infrastructure using modern AI-assisted tools.

The Medical Writer supports the development of CE-certified initiatives by translating complex scientific and clinical information into clear, engaging, and compliant content, while also assisting with grant proposals. Responsibilities include developing therapeutic area knowledge, reviewing and editing various content formats, conducting literature reviews, and ensuring adherence to regulatory and editorial standards.

The role involves developing high-quality, evidence-based medical communications content, including advisory board materials, training resources, and scientific messaging for various channels. Responsibilities also include ensuring all content is scientifically accurate, properly annotated with references, and compliant with regulatory standards.

The role involves developing high-quality, scientifically rigorous content for peer-reviewed publications and congress deliverables, partnering with Medical Affairs teams and KOLs to translate complex clinical data into clear communications. Responsibilities include writing and editing manuscripts, abstracts, and posters, ensuring all materials adhere to compliance guidelines like ICMJE and GPP.

The Scientific Director will primarily utilize clinical expertise to analyze and interpret oncology data to craft educational content for live events and sponsored videos, ensuring projects meet high standards from conception through delivery. Responsibilities also include leading diverse projects, interfacing with clients and key opinion leaders, and providing training and mentorship to direct reports like Medical Writers and Editors.