In this role, you will serve as a Site Alliance Relationship Manager for assigned Sites across a variety of site models, supporting Parexel Site Alliance Strategy, managing quality, performance, analyzing metrics, and identifying opportunities and challenges. Job Duties: Strategy and Metrics * Regularly analyzes site performance and utilization data. * Ensures GCP and SOP compliance at site and measure Key Performance Indicators of assigned Alliance Sites and manage/escalate performance issues. * Participate in the development of Parexel Site Strategy in both Pre and Post Award opportunities. * Establish metrics aligned with corporate, team and individual goals and provide regular output to VP, Global Site Alliances. Site Relationship Management * Maintain Site Profiling data to ensure the right studies are mapped to the right sites. * Support site throughout clinical trial journey to ensure accountability for site meeting/exceeding study deliverables. * Initiates action plans to improve efficiencies, project outcomes and quality metrics for operation processes and roles. * Ensures continuous improvement of processes applied by the Alliance Sites to execute on trials. * Develops, aligns, and maintains processes (SOP) and RACI with special emphasis on Feasibility, Study Start-Up, Patient Recruitment and Site Management. * Engage cross-functionally to effectively identify clinical trial opportunities based on the site profiling capabilities. Skills required: * Ability to analyze metrics and information to ensure activities and decisions are informed by data analysis. * Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines. * Good written and verbal communication skills, effective presentation skills, and asks questions to identify needs and issues. * Good organizational and time management skills and ability to manage competing priorities. * Demonstrates flexibility in respect to work assignments, interacting with others, and new learning. Ability to think and act innovatively and creatively with strong focus on execution. * Takes appropriate actions to escalate issues as needed in compliance with Parexel's SOP's. * Takes responsibility for decision making and for his/her performance and delivery. * Proficiency in use of Microsoft Word, Excel and PowerPoint. * The ability to travel up to 30%. * Competent in written and oral English. Fluent in local language where required, as an example for example, Spanish, French, German, Mandarin or Japanese. Knowledge and Experience required: * In depth knowledge of the drug development processes across all functional areas. * Minimum of 2 years of experience in the conduct of clinical trials from the pharmaceutical industry, CRO business or from a clinical background; or equivalent combination of education, training and experience. Education: * Educated to a degree level in biological science, pharmaceutical science or other health related discipline or other relevant clinical or business equivalent education. * A Bachelor of Science or Bachelor of Art degree or equivalent work experience.
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EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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