At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.
What we offer:
- Competitive compensation + shift allowances
- Attractive benefits (security, flexibility, support, and well-being)
- Engaging employee programs
- Technology for hybrid working and great onsite facilities
What you’ll be doing:
- The Medical Writer is responsible for working with the Statistical and Scientific teams to create Expert Reports and Statistical Analysis Plans as well as assist with synopsis and protocol development.
- Create, edit/proofread, and finalize Expert Reports based on the output of the statistical analysis (Tables, Listings, and Figures) and the final conclusions of the Scientific team.
- Work with the Statistical team to create, edit/proofread, and finalize the Statistical Analysis Plan(s).
- Work with the Statistical and Scientific teams to help sponsors with the development of synopsis and protocols for the cardiac safety component.
- Overall management of timelines of all deliverables in terms of Expert Reports, Statistical Analysis Plans, and other outputs as needed.
- Understand FDA/EMA regulations in regards to clinical trial reporting.
What we look for:
- Bachelor’s Degree in Science or Healthcare related field
- At least five years of previous experience in medical or scientific writing for publications, reports, or grant submissions
- Excellent English language skills (writing, reading, verbal)
- Knowledge of clinical trials environment and regulations
