Medical Writer II (Clinical Trial Transparency)

About the role

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals.

What you'll do

• Mentors less experienced medical writers on projects, as necessary
• Compiles, writes, and edits medical writing deliverables, and serves as a medical writer within and across departments with minimal supervision
• Develops or supports a variety of documents that include but not limited to: o Clinical study protocols and clinical study protocol amendments; o Clinical study reports
• Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency
• Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables

What you need

• 1–3 yrs of experience
• Clinical research
• Regulatory affairs
• SOP writing
• Customer success
• Any graduate