When our values align, there's no limit to what we can achieve.
Parexel is in the business of improving the world's health.
We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments.
We believe in our values,This role can be either fully remote or office based in any of the following countries: UK, Ireland, You can choose the right working arrangement for you, your role, and your location — in the office, home-based or a mix!
Our offices are open planned, and you will be working in an innovative and collaborative environment with your international peers and colleagues.As the , you will be assigned to Sites across a variety of site models, supporting Parexel Site Solutions Strategy, managing quality, performance, analyzing metrics, and identifying opportunities and challenges.Key Accountabilities:Strategy and MetricsRegularly 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 AlliancesSite Relationship ManagementMaintain 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.Education:Educated to a degree level in Biological Science, Pharmaceutical Science or other health related disciplines or other relevant clinical or business equivalent education.A Bachelor of Science or Bachelor of Art degree or equivalent work experience.Skills: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 10% - 30%.Competent in written and oral English.
Knowledge and Experience:In depth knowledge of the drug development processes across all functional areas.Advanced 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.In return we will be able to offer you a structured career pathway and encouragement to develop within the role including awareness and understanding of the industry.
You will be well supported and for your hard work you will be rewarded with a competitive base salary as well as a benefits package including holiday as well as other benefits that you would expect with a top company in the CRO Industry.
