Description Why Syneos Health? Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most. Evolve in a global company that is always looking for ways to work smarter and more efficiently as the only fully integrated Biopharmaceutical Accelerator. You'll be supported with comprehensive resources based on today's emerging technologies, data, science and knowledge - instead of practices from the past. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment to over-deliver and outperform. A career with Syneos Health means your everyday work improves patients’ lives around the world We are looking for Manager, Safety/Pharmacovigilance responsible for the team of Safety Specialists to be based in the UK, Camberley. A brief summary of duties you will be involved in as a Manager, Safety/Pharmacovigilance: •Line management responsibilities including transfers, hiring, utilization, terminations, training, professional development, performance appraisals, job description preparation, time sheet approval, and employee counseling. •Assigning project work and reviews workload for all direct reports. Providing oversight and guidance on organizational goals and company objectives. •Monitoring quality of work and efficiency of team members with contracted scope of work and Safety Management Plan. Discussing below-target project goals with Associate Director/Director/VP. •Managing projects where Safety and Pharmacovigilance are the primary services: ◦Reviews study budgets and expenses; ensures all study related contractual and budgeting issues are upheld and performed. ◦Works with Finance to ensure appropriate customer invoicing, where required. ◦Approves project time cards and invoicing. ◦Provides sponsors with scheduled project updates and reports. •Participates in the management of the Safety and Pharmacovigilance department with the following actions: ◦Assists in the development, review, and approval of departmental Standard Operating Procedures (SOPs) or ensures compliance with sponsor SOPs. ◦Ensures the execution of the Safety Management Plan/Safety Reporting Plan. ◦Evaluates processes for potential improvement in efficiency and effectiveness and recommends changes. Participates in process development and improvement of departmental functions. •Works with Business Development to actively solicit new business, as needed. •Reviews, advises, and approves drug safety portions of project proposals to ensure wording adequately reflects the scope of work for drug safety. Reviews and approves clinical safety sections of study protocols and Case Report Forms (CRFs). Approves budget projections for the project. •Maintains understanding of SOPs, Work Instructions (WIs), global drug/biologic/device regulations, GCPs, ICH guidelines, and the drug development process. . Qualifications Skills and attributes: BA/BS in the biological sciences or related disciplines in the natural science/health care field or nursing degree. Moderate clinical research/drug safety experience or an equivalent combination of education and experience. Progressive responsibility with demonstrated leadership skills. Clinical Research Organization (CRO) experience with therapeutic specialties preferred. Working knowledge of financial budgets and various financial analysis tools preferred. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, MS Project), email, and internet. Excellent oral, written, and interpersonal communication skills with strong graphic presentation skills. Ability to be flexible, adapt to change, work independently, as well as part of a team in a matrix environment. Ability to make effective decisions and manage multiple priorities while delivering high quality work in a dynamic environment. What happens next: If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity. 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 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. 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.