Senior Medical Writer - Early Phase (Single Sponsor Support)
5 hours ago
Madrid
ppSenior Medical Writer - Early Phase (Single Sponsor Support) 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. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. 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 deliver – for one another, our customers, and, most importantly, for those in need. /ppDiscover what your 25,000 future colleagues already know. /ph3Why Syneos Health /h3ulliWe are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. /liliWe are committed to building an inclusive culture – where you can authentically be yourself. /liliCentral to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. /liliWe are continuously building the company we all want to work for and our customers want to work with. /li /ulh3Job Responsibilities /h3ulliLeads the clear and accurate completion of medical writing deliverables, ensuring scientific information is presented clearly and accurately. /liliManages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. /liliLeads the resolution of comments from the client. /liliCompletes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; 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. /liliAdheres 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, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget. /liliCoordinates quality and editorial reviews. /liliEnsures source documentation is managed appropriately. /liliLeads team document reviews, and reviews documents as needed. /liliActs as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format. /liliReviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency. /liliProvides feedback to further define statistical output required and document needs. /liliInteracts and builds good working relations with clients, department head, and peers in data management, biostatistics, regulatory affairs, and medical affairs, as necessary, to produce writing deliverables. /liliPerforms online clinical literature searches and complies with copyright requirements. /liliIdentifies and proposes solutions to resolve issues, escalating as appropriate. /liliProvides technical support, training, and consultation to department and other company staff. /liliMay contribute to development of internal materials and presentations or changes to internal process, standard practices, and capabilities. /liliMentors and leads less experienced medical writers on complex projects, as necessary. /liliDevelops deep expertise on key topics in the industry and the regulatory requirements and guidelines that affect medical writing. /liliAware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership. /liliCompletes required administrative tasks within the specified timeframes. /liliPerforms other work-related duties as assigned. /liliMinimal travel may be required (less than 25%). /li /ulh3Qualifications /h3ulli3-5 years of relevant experience in regulatory writing. /liliExperience working in the biopharmaceutical, device, or contract research organization industry required. /liliStrong understanding of EMA, FDA and ICH regulations, other regulatory guidelines, and/or good publication practices strongly required. /liliExperience writing relevant document types required. /liliExtensive knowledge of English grammar and ability to communicate clearly; strong familiarity with AMA Manual of Style. /li /ulh3Get to know Syneos Health /h3pOver the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. /ppLearn more about Syneos Health. /ph3Additional Information /h3pTasks, 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. /ppOccasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. 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. /ppDiscover what our Syneos Health colleagues already know: work here matters everywhere. Work alongside the brightest minds in the biopharmaceutical industry taking down walls and removing barriers to speed our customers’ delivery of important therapies to patients. We are strategic thinkers who actively seek different perspectives, whether across offices or across oceans. Because we solve some of the toughest challenges facing the most prestigious healthcare companies today, you'll gain exposure and be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. The diversification and breadth of Syneos Health creates a multitude of career paths and employment opportunities. We’re a growing, global company dedicated to advancing our talent past their initial role. Discover what our 29,000 employees already know: work here matters everywhere. We work hard, and smart, all in the name of getting much-needed therapies to those who need them most. A career with Syneos Health means your everyday work improves patients’ lives around the world. Selecting us as an employer secures a career in which you’re guaranteed to: Partner with the most diverse team of experts in the industry. From the top down, our people are inspiring. Everyone has a voice and is encouraged to use it. Work in specialized Syneos Health teams that are therapeutically or functionally aligned for expert collaboration. We assemble clinical teams where everyone, from CRAs to senior management, is skilled in the same therapeutic area or customer teams. With this structure, everyone on your team speaks the same language and can deliver unique insights into the therapeutic environment and patient population. We are partners with purpose. We integrate seamlessly with our customers and do what’s best for their success. Our people provide the brilliant ideas, valuable insights and endless energy that accelerates the impact of life changing therapies worldwide. /p /p #J-18808-Ljbffr