Sr. Medical Writer (Regulatory)

Updated : April 3, 2026 Location : Morrisville, NC, United States Job ID : 25104252 Company Overview Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Job Responsibilities Leads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Leads the resolution of comments from the client. Completes a variety of documents that may include clinical study protocols and protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; plain language summaries; periodic safety update reports; clinical development plans; IND submissions; integrated summary reports; NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings. Adheres to established regulatory standards, including ICH E3 guidelines, company standard operating procedures, client standards, and approved templates, authorship requirements, and style and formatting guides, completing projects on time and on budget. Coordinates quality and editorial reviews, ensures source documentation is managed appropriately, leads team document reviews, and reviews documents as needed. Acts as peer reviewer for internal team to ensure scientific content, clarity, overall consistency, and proper format. Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, grammar, format, and consistency; provides feedback to further define statistical output required and document needs. Interacts and builds good working relations with clients, department heads, and peers in data management, biostatistics, regulatory affairs, and medical affairs to produce deliverables. Performs online clinical literature searches and complies with copyright requirements. Identifies and proposes solutions to resolve issues, escalating as appropriate; provides technical support, training, and consultation to department and other company staff; may contribute to development of internal materials and presentations or changes to internal processes, standard practices, and capabilities. Mentors and leads less experienced medical writers on complex projects. Develops deep expertise on key topics in the industry and the regulatory requirements and guidelines that affect medical writing. Is aware of budget specifications for assigned projects, works within the budgeted hours, and communicates status and changes to medical writing leadership. Completes required administrative tasks within specified timeframes. Performs other work-related duties as assigned. Minimal travel may be required (less than 25%). Benefits Company car or car allowance Health benefits, including medical, dental, and vision Company match 401(k) Eligibility to participate in Employee Stock Purchase Plan Eligibility to earn commissions/bonus based on company and individual performance Flexible paid time off (PTO) and sick time (subject to state and municipal regulations) Salary Range $80,600.00 - $145,000.00 Additional Information 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 incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. #J-18808-Ljbffr