At Clario, we are committed to transforming clinical trials through technology and innovation. As aMedical 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.