Medical Writer

At Clario, we are committed to transforming clinical trials through technology and innovation. As a Medical Writer, you’ll play a pivotal role in shaping high-quality clinical documentation that supports critical research and regulatory success. This position ensures clarity, compliance, and excellence in our clinical studies—directly impacting patient outcomes and organizational goals. If you’re detail-oriented and passionate about medical writing, this is an opportunity to grow your career while contributing to meaningful work in global healthcare.

What We Offer

• Competitive compensation
• Private health insurance
• Flexible work schedules
• Attractive paid time off plan
• Engaging employee programs

What You’ll Be Doing

• Review study protocols for inclusion/exclusion criteria, imaging objectives, endpoints, and indication-specific requirements
• Review study-specific electronic Case Report Forms (eCRFs/CRFs)
• Create and finalize Charters, Clinical Data Transfer Plans (CDTPs), and Reader Training Packages (RTPs)
• Draft compliance reports including Notes to File, Corrections, Transfer of Obligations, and deviation reports
• Review and update Investigator Meeting slides and SOPs related to Medical Communications
• Supervise Associate Medical Writers and maintain MedComm web pages
• Update training modules and ensure consistency across study start-up documents
• Manage document development lifecycle, including CRs, tracking databases, and template updates
• Provide guidance to project teams and ensure timely delivery of final effective documents
• Participate in internal and external meetings related to study documentation
• Stay current on response criteria publications and participate in training activities

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 in pharmaceutical, clinical, or imaging research required
• Proficiency in medical, regulatory, and clinical writing
• Strong command of MS Office Suite
• Familiarity with clinical trial terminology
• Excellent attention to detail, documentation, and organizational skills
• Strong communication and interpersonal abilities
• Ability to manage multiple projects and adapt to changing priorities
• Experience with long-duration computer work; minimal travel (0–5%)

At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.