Review study protocols and contracts for inclusion/exclusion criteria, imaging objectives, endpoints, and indication‑specific requirements
Review study‑specific electronic Case Report Forms (eCRFs/CRFs) for accuracy and alignment with protocol requirements
Develop, write, and finalize study documentation including Site Manuals, Quick Reference Guides, Charters, and other study‑related documents or forms as requested
Review, update, and support Standard Operating Procedures (SOPs) related to Medical Communications
Manage the document development lifecycle, including version control, tracking databases, and template maintenance
Provide guidance to project teams to ensure timely delivery of final, approved documentation
Participate in internal and external meetings related to study documentation and deliverables
Ensure all documentation meets quality, regulatory, and internal compliance standards
Maintain accurate and organized documentation records in accordance with company policies
What We Look For
Bachelor's degree in Life or Physical Sciences (e.g., Biology, Chemistry, Pharmaceutics)
2+ years of medical writing experience preferred
3+ years of experience in pharmaceutical, clinical, or imaging research environments required
Proficiency in medical, regulatory, and clinical writing
Strong working knowledge of clinical trial terminology and documentation standards
Proficiency with Microsoft Office Suite
Excellent attention to detail, documentation, and organizational skills
Strong written and verbal communication and interpersonal skills
Ability to manage multiple projects, prioritize effectively, and adapt to changing timelines
Ability to perform long‑duration computer‑based work
Minimal travel required (approximately 0-5%)
Benefits
Competitive compensationComprehensive health and wellness benefitsFlexible work arrangementsPaid time off and company holidaysEngaging employee programs and professional development opportunitiesHealth insuranceFlexible schedule
Additional Information
At Clario, a part of Thermo Fisher Scientific, we are committed to transforming clinical trials through technology and innovation. As a Medical Writer, you will play a pivotal role in developing high‑quality clinical documentation that supports critical research and regulatory success. This position ensures clarity, consistency, and compliance across clinical studies, directly impacting patient outcomes and organizational goals.
Clarioclinical · Remote