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Medix™

Clinical Writer - 119425

Medix™, Union, New Jersey, United States


Medical Writer Job Description As a medical writer, you will be responsible for writing documents, articles, journals, brochures, and product manuals for our organization. You will cover topics in clinical trials, treatments, procedures, medical devices, pharmaceutical drugs, medical research/breakthroughs, and other educational materials. Roles and Responsibilities Write and edit high-quality medical journals, abstracts, white papers, articles, brochures, regulatory documents, and product manuals about healthcare-related topics such as [new medicinal discoveries/treatments, educational materials, clinical research, and product instructions]. Communicate with medical experts, patients, or representatives from pharmaceutical companies for medical resources and verifications. Conduct research on [treatments, illnesses, diseases, pharmaceutical drugs, clinical studies, and medical products]. Create content calendars and timelines for our website, newsletters, and PR. Conduct interviews with subject matter experts, healthcare thought leaders and providers about medical breakthroughs. Identify industry trends by reviewing related literature searches. Collaborate and verify data with our internal study team. Thoroughly study reports and cross-check information. Conduct frequent and thorough quality control checks on each submission. Ensure that documents adheres to the organization’s writing guidelines, and are appropriately stored and organized. Skills Broad & In-Depth Expertise in Clinical Concepts and Regulations Journalism Technical Writing Analytical Thinking Critical Thinking Literature Research Data Interpretation Project Management Medical Communications Qualifications A Bachelor’s Degree in journalism, English, life science, biology, research, statistics, or any related field.