Job Description

Description Manager, Medical Editing Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their objectives. 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 to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE Why Syneos Health We 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. We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we arededicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why Because when we bring togetherdiversity of thoughts, backgrounds, cultures, and perspectives - we\'re able to create a place where everyone feels like they belong. Job responsibilities . Supervises staff and oversees development of direct reports by setting goals, conducting performance reviews, evaluating and monitoring training needs, creating development plans, mentoring, and coaching . Sets priorities, schedules department resources, implements company objectives, and creates alternative solutions to address business and operational goals . Recommends courses of action on salary administration, interviewing and selection, terminations, professional development, performance appraisals, job description preparation, and employee counseling . Works with and advises staff on administrative policies and procedures, technical problems, priorities, and methods . Manages and oversees the editing, data integrity review, and/or publishing of medical writing deliverables per company or client standard operating procedures . Reviews department work products for completeness, accuracy, and overall quality assumes responsibility for quality of department work products . Serves as primary point of support to and liaison with the company\'s medical writing leadership team on editorial, data integrity review, and/or electronic publishing issues . Assists with or performs budgeting, revenue recognition, invoicing, and forecasting . Assists with timeline creation for medical writing deliverables . Edits, proofreads, performs data integrity review for, and/or publishes regulatory, commercialization, and medical information documents as required . Develops and maintains department standard operating procedures . Builds and maintains relationships with internal and external customers . Assists in tracking, maintaining, and reviewing department metrics . Supports business development activities by assisting with proposal and costing development, as well as bid defense and customer meetings Qualifications What we\'re looking for . Bachelor\'s degree (preferred) in the life sciences, clinical sciences, or English/journalism or copyediting, data integrity review, and/or relevant publishing experience. . Looking for Min 8 yrs of experience into scientific or Regulatory Writing & 2 years into people management. . Experience in Line management, Project management and Client management. Exposure into Project management and Client management (handling multiple clients). . Management experience preferred, including senior-level or team-lead experience in medical/technical editing and/or electronic publishing within the pharmaceutical, biotechnology, medical education, medical publishing, or contract research organization industries. . Extensive knowledge of English grammar FDA, EU, ICH and ISO regulations and guidelines governing drug/device and document development and editorial and publications processes, systems, procedures, and best practices. . Familiarity with principles of clinical research. . Track record of successful relationship building with internal and external customers, including an ability to motivate others and build teams. . Ability to supervise and train employees and to organize, prioritize, and schedule work assignments. Strong management and independent work skills strong written composition and editorial skills and program planning and implementation skills. . Excellent communication, presentation, and interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade. . Demonstrated team-oriented approach. Strong Microsoft Office Suite skills. Get to know Syneos Health Over 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. Learn more about 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 . 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. Occasionally, 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.

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