Clario, a part of Thermo Fisher Scientific, is a global leader in endpoint data solutions for clinical trials. With more than five decades of experience, the company combines deep scientific expertise with cutting‑edge imaging, eCOA, motion, cardiac and respiratory technologies to generate high‑quality clinical evidence. Over 30,000 trials across 100+ countries have benefited from Clario’s solutions, contributing to more than 70% of FDA drug approvals since 2015. The organization’s purpose – to transform lives by unlocking better evidence – drives a culture of innovation, collaboration and relentless focus on patient outcomes. The Associate Medical Writer role sits within the Medical Imaging team and offers a unique entry point for fresh talent eager to build a career at the intersection of medical writing, clinical research operations and imaging science. Reporting to senior medical writers and project leads, you will be responsible for creating, reviewing and maintaining a wide range of study‑specific documentation that underpins successful trial execution. This position provides exposure to cross‑functional teams, regulatory standards and real‑world clinical data, making it an ideal springboard for a long‑term career in medical communications or clinical operations. Key Responsibilities: 1. Support study startup by drafting, organizing and curating Medical Writing and Communications documents such as Site Manuals, labels and study‑specific forms. 2. Review protocols and imaging requirements to ensure accurate interpretation of procedures, schedules and operational needs. 3. Create, update and finalize study documentation, including supporting forms, labels, and communication materials. 4. Develop and maintain compliance artefacts like Notes to File, amendment impact assessments and corrective action records. 5. Generate source documentation and electronic clinical forms that align with operational requirements. 6. Prepare meeting agendas, minutes and action‑item logs for study startup and project meetings. 7. Assist in maintaining Medical Communications resources, databases, web content and document repositories. 8. Participate in project close‑out activities, ensuring proper archiving per regulatory and company standards. 9. Contribute to SOPs, work instructions, templates and training material development. 10. Track document status, maintain databases and provide guidance to project teams on documentation processes. Technical Stack & Tools: Microsoft Office Suite (Word, Excel, PowerPoint, Outlook), electronic document management systems, clinical trial management systems (CTMS), basic knowledge of imaging software and regulatory submission platforms. Growth Path: Starting as an Associate Medical Writer, you can progress to Senior Medical Writer, Lead Medical Writer, and eventually to Medical Communications Manager or Clinical Operations Lead, with opportunities to specialize in imaging, regulatory affairs or therapeutic areas. Why Join Clario? You will work alongside world‑class scientists and technologists, gain hands‑on experience with high‑impact clinical studies, and benefit from a supportive environment that encourages continuous learning, professional certifications and global mobility. The blend of competitive compensation, flexible remote‑work options and a clear career roadmap makes Clario an attractive destination for ambitious freshers.