Medical Writer (Clinical Trail Transparency)

Role & responsibilities:

•    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;     o    Patient narratives;     o    Annual reports;     o    Investigator brochures.•    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. •    Serves as peer reviewer on internal review team. Addresses team comments accurately to ensure document scientific content, clarity, overall consistency, and proper format.•    Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.•    Performs on-line clinical literature searches, as applicable. •    Working knowledge of drug development process and regulatory guidelines.•    Continues professional development to keep pace with regulatory guidance and client expectations in medical writing that affect medical writing.•    Stays aware of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.•    Completes required administrated tasks within the specified timeframes.•    Performs other work-related duties as assigned.