Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred 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 Summary The Principal Medical Writer I is responsible for the development of clinical documents for submissions to regulatory authorities globally. Job Responsibilities - Provides strategic direction to cross-functional project teams with minimal oversight to ensure that clinical documents (e.g., Investigators' Brochures [IBs], Clinical Study Reports [CSRs], and marketing authorization submission documents) accurately and consistently present key data-driven clinical messages in accordance with program goals and regulatory requirements. - Writes or provides direction and leadership to other writers to ensure the timely delivery of high quality documents that are scientifically rigorous, logically organized, and have accurate data presentation and interpretation. - Oversees the medical writing activities of multiple compounds and serves as lead writer for individual summary documents. - Has a broad understanding of clinical research processes and global regulatory document standards. - Mentors less experienced writers. - Reports to a Director of Medical Writing or above. Responsibilities - Develop regulatory documents for submission to regulatory agencies globally, in accordance with ICH and other global guidelines, standards and processes, and the client authoring standards, as applicable, in adherence with study/project timelines and corporate objectives. - Manage medical writing projects, including developing timelines (working with the study/project teams, as necessary) and communication with cross-functional team members to maintain awareness of review cycles and expectations. - Participate in cross-functional meetings to provide input regarding medical writing deliverables, timelines, and any process(es) needed for the completion of regulatory documents. - Review other documents associated with the assigned project(s) (e.g., Protocols and Statistical Analysis Plans), as appropriate. - Participate in cross-functional process improvement initiatives. - Participate in defining and writing standard operating procedures and best practices for an efficient preparation of quality documents. - Manage internal and contract medical writing resources as required to ensure timely completion of assigned projects. - Mentor more junior medical writing staff. Minimum Requirements and Competencies - Bachelor's degree required. Advanced degree in a relevant scientific/clinical/regulatory field preferred. - At least 5 years of medical writing experience in the biopharmaceutical/CRO industry required or comparable experience within clinical or preclinical development. - Proficiency in organizing and communicating clinical information required with minimal oversight. - Strong organizational, time management, and project management skills are required. - Strong verbal, written, and interpersonal communication skills needed to work effectively in a team environment. - Proficient understanding and knowledge of global regulatory requirements needed and knowledge of therapeutic areas in all phases of clinical development desired. - Proficient in MS Word. Experience with an electronic document management system and templates is required. Benefits At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all appl