Description Senior Medical Writer 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.
Our Clinical Development model brings the customer and the patient to the center of everything that we do.
We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
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.
We are agile and driven to accelerate the delivery of therapies because we are passionate about changing lives.
Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE.
Job ResponsibilitiesMentors and leads less experienced medical writers on complex projects, as necessary.Acts as lead for assigned writing projects.Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision.Develops or supports a variety of documents that include, but are not limited to: clinical study protocols and clinical protocol amendments; clinical study reports; patient narratives; clinical development plans; IND submissions and annual reports; integrated summary reports; NDA and (e)CTD submissions; investigator brochures; clinical journal manuscripts; clinical journal abstracts; and client presentations.Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, 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 providing review comments on draft and final documents.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 online clinical literature searches, as applicable.Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.Completes required administrative tasks within the specified timeframes.Performs other work-related duties as assigned.
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