Draft and copyedit submissions for abstracts, posters and peer-reviewed manuscripts.
Work collaboratively with other team members and actively participate in pub planning activities.
Perform fact/data check on writing documents (manuscripts, white papers, dossiers, etc.).
Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. The Natera team consists of highly dedicated professionals from world-class institutions, who care deeply for our work and each other.
Plays an essential role supporting Global Medical Information / Medical Content Development Team on content development-related engagements.
Writes and creates medical and scientific content related to Medical Affairs, Medical Information and Medical Communications.
Drives the client document development process from gathering materials and developing scientifically rigorous content to facilitating document review.
EVERSANA delivers next-generation commercialization services to the life sciences industry, helping bring innovative therapies to market and supporting patients. They have over 6,000 employees, embracing diversity and inclusion to improve patient lives around the world.
Write promotional content such as ad copy, headlines, questionnaires, emails, and landing page text to improve click-through rates and signups for clinical trial recruitment campaigns.
Translate complex medical information from trial protocols into clear, engaging, and patient-friendly messaging while maintaining accuracy.
Revise copy based on feedback and campaign data, conduct QA scoring, and contribute to improving templates and workflows for better performance.
Trialfacts recruits participants for clinical trials, connecting academic researchers and commercial sponsors with the right people for their studies. It is a 19-year-old company with 35 team members across 7 countries, operating with a mission-driven culture focused on accelerating health research.
Preparation of Initial Investigational New Drug (IND) applications and amendments.
Provide guidance and support to other in‑house units in the preparation or review of manuals, training guidelines, and similar documentation.
Serve as a resource for new medical writers, offering direction, feedback, and support as needed.
Theradex Oncology is a full-service CRO, conducting early and late-phase oncology trials in the U.S, Europe and Asia. Their focus is cancer, understanding the science behind each potential cancer therapy and the challenges of moving therapies from mice to man.
Author, review, and manage clinical, regulatory, technical, and medical documents including protocols, study reports, and regulatory submissions.
Ensure strategic alignment and consistency of scientific messaging across documents while maintaining compliance with global regulatory requirements.
Drive the end-to-end writing process, manage timelines, and lead cross-functional reviews to deliver high-quality, on-time deliverables.
Kiniksa Pharmaceuticals is a commercial-stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, focusing on cardiovascular indications. The company fosters a highly collaborative, patient-first culture led by accomplished life sciences leaders, empowering talented individuals to make a real impact.
Review and edit promotional content/materials for grammar and consistency.
Fact check/Cross-check and proofread existing content.
Retain medical, legal, and regulatory guidance to ensure consistency and accuracy.
P10 was born of the idea that if something isn’t working—or could work better—change it. P10 brings together a team of diverse, remote-only seasoned professionals to deliver exceptional value for clients.
Responsible for planning, development, and oversight of scientific content.
Provide clients with strategic medical communication recommendations.
Independently lead execution of content development activities.
Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to identify effective, holistic, science-based strategies through medical communications. Over a third of their staff hold advanced scientific or medical degrees, and most work from where they live.
Develop client-ready deliverables such as study protocols, statistical analysis plans, and technical reports for health technology assessment submissions.
Manage project components by collaborating with team members to ensure timely delivery, financial performance, and high-quality outputs, while handling day-to-day client communications.
Provide mentorship and direction to junior researchers, contribute to business development proposals, and apply technical expertise in systematic reviews and indirect treatment comparisons like NMA and MAIC.
Precision Medicine Group is a global portfolio organization specializing in evidence synthesis for health technology assessments in the pharmaceutical industry. The company has a culture similar to a start-up, is well-funded, and prides itself on being a visionary leader in its field.
Develop client-ready deliverables including protocols, statistical analysis plans, and technical reports.
Manage the delivery of project components by collaborating with other staff members.
Contribute to development of proposals and presentations under guidance of senior team members.
Precision Medicine Group is a portfolio organization that helps its clients with sophisticated evidence synthesis projects. The company has a start-up culture with vision in its field.