**Description****Senior/Principal Medical Writer**Come discover what our 25,000+ employees already know: work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you- ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of.As a part of the Syneos Health team, you’ll help us deliver results for a rewarding reason – we improve patients’ lives around the world. Because to us, a patient isn’t just a number, they’re our family, friends, and neighbors.**Why Syneos Health**- #SyneosHealthLife means we’re committed to our Total Self culture – where everyone can authentically be themselves.
Our Total Self culture is what unites us globally, and we know every person’s unique contributions make a difference.- We believe our success is a direct result of the people who are driving it – you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That’s why we offer a comprehensive benefits program encompassing your total health – physical, mental and financial.- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.**JOB SUMMARY**:Syneos Health is looking for a Senior/Principal Medical Writer to join our organization. This is a permanent and fully remote role and it is open across Europe. The role serves as a senior medical writer on clinical study or regulatory project teams. Writes, edits,
and coordinates content for clinical/regulatory while serving as primary technical contact with the internal team and the client.**JOB RESPONSIBILITIES**:- Mentors 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 mínimal supervision.- Develops or supports a variety of documents that include, but 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, as well as; – 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, 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 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 on-line 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 administrated tasks within the specified timeframes.- Performs other work-related duties as assigned. Minimal travel may be required (less than 25%).**Qualifications**QUALIFICATION REQUIREMENTS- Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree (Social Sciences, English or Communications, preferred)
with relevant scientific and/or medical knowledge and expertise.- Extensive knowledge of English grammar and FDA and ICH regulations and guidelines as well as a familiarity with AMA style guide.- Demonstrated high degree of independence with effective presentation, proofreading, interpersonal, and leadership skills and ensure a team-oriented approach.- Ability to demonstrate a familiarity with principles of clinical research and to interpret and present clinical data and other complex information.**Disclaimer**:Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of
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