Each day, you’ll be reminded about why you chose a career in healthcare. The work is challenging. The pace is exhilarating. The people – your colleagues and our customers – are inspiring. Unlike traditional CROs and commercialization businesses, at Syneos Health we are purpose-built to see the big picture. Our uniquely integrated approach to bringing new therapies to market means you will work in sync with colleagues across clinical and commercial disciplines to share data, insights and knowledge. Grow your career with a global company that is taking down walls and removing barriers to achieve one goal: shortening the distance from lab to life® ROLE: The Senior Pharmacokineticist will provides guidance on the efficient execution and analysis of bioequivalence and pharmacokinetic studies consistent with accepted industry standards. The work location can be in Quebec City, Montreal, Toronto or Home Based. TASKS AND RESPONSIBILITIES : Conducts, participates in, and/or manages activities related to pharmacokinetics in the design, implementation, data analysis, summarization, and reporting of clinical trials. Participates in Sponsor meetings and advises on pharmacokinetic analysis. Provides training on pharmacokinetic analysis by developing training courses, presenting training materials, mentoring new associates, reviewing their work, and providing feedback. Mentors other pharmacokineticists and department staff. Critically reviews and evaluates the scientific merit of potential projects. Conducts literature reviews and provides scientific support for assigned projects including complex scientific projects. Advises supervisors, colleagues, and other departments in areas of expertise. Provides extensive input on study design. Designs and writes or reviews concept protocols, full protocols, and informed consents. Writes and reviews Statistical Analysis Plans based on the protocol and develops organized mock-up displays for tables, listings and figures adhering to the SAP in collaboration with the Biostatistician. Writes and reviews project reports, expert opinions, and investigator brochures. Prepares abstracts, papers, and manuscripts for publication or presentation. Participates in national and international scientific meetings as appropriate. May act as team leader and/or project manager for combined consulting/clinical research projects, coordinating assigned resources, and communicating with sponsor. Directs the work of other professional staff in the accomplishment of assigned goals and assist in training, development, and evaluation activities. Participates in business development activities as required. REQUIREMENTS : Master’s degree in Science, 4 years of experience or Ph. D, 2 years of experience in a similar position in pharma industries or CRO. An equivalent combination of education, training and experience can be considered Appropriate communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade. In-depth understanding and knowledge of the pharmaceutical industry and contract research organizations in general, and the clinical community specifically Experience with software Phoenix WinNonlin English level: Required English proficiency includes being able to communicate verbally on subjects that are frequently scientific and specialized. Other (optional): Candidate who does not possess the required training and/or experience may be considered under different criteria.